HIV molecular immunology database
Found 4 matching records:
HXB2 Location | Gag(147-155) | Gag Epitope Map
View variants at this location |
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Epitope |
ISPRTLNAW
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Epitope Alignment | ||||||||||||||||||||||||||||
Variants |
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Epitope Name | ISW9 | |||||||||||||||||||||||||||||
Species (MHC/HLA) | human(B*57:01) |
Showing all: 9 variant(s).
Variant ID. | 3172 |
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Epitope Seq. | {A}ISPRTLNAW |
Variant Seq. | {s}lSPRTLNAW |
Mutations | A/S I/L |
Epitope Location | A-1S I1L |
HXB2 Location | A145S I146L |
Mutation Type | OV: observed variant |
Epitope Subtype | B |
Variant Subtype | B |
Method | Sequence |
Note | Flanking and epitope mutations, {s}lSPRTLNAW{V}, were seen for ISW9 by 13 weeks post-infection in patient 1 (P1) who carried HLA alleles A*0101, A*0301, B*2705, B*5701. |
Variant ID. | 3173 |
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Epitope Seq. | {A}ISPRTLNAW |
Variant Seq. | {p}lSPRTLNAW |
Mutations | A/P I/L |
Epitope Location | A-1P I1L |
HXB2 Location | A145P I146L |
Mutation Type | OV: observed variant |
Epitope Subtype | B |
Variant Subtype | B |
Method | Sequence |
Note | Flanking and epitope mutations, {p}lSPRTLNAW{V}, were seen for ISW9 by 104 weeks post-infection in patient 1 (P1) who carried HLA alleles A*0101, A*0301, B*2705, B*5701 and at 179 weeks post-infection in patient 3 (P3) who carried HLA alleles A*2402 , A*3201, B*4002, B*5701. |
Variant ID. | 3174 |
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Epitope Seq. | ISPRTLNAW |
Variant Seq. | lSPRTLNAW |
Mutations | I/L |
Epitope Location | I1L |
HXB2 Location | I146L |
Mutation Type | OV: observed variant |
Epitope Subtype | B |
Variant Subtype | B |
Method | Sequence |
Note | Epitope mutation, A|lSPRTLNAW|V, was seen for ISW9 by 271 weeks post-infection in patient 1 (P1) who carried HLA alleles A*0101, A*0301, B*2705, B*5701; at 45 weeks post-infection in patient 3 (P3) who carried HLA alleles A*2402 , A*3201, B*4002, B*5701; from 144 weeks post-infection in patient 5 (P5) who carried alleles A*0101,A*0101,B*0801,B*5701 and from 17 weeks post-infection in patient 6 (P6) who carried alleles A*0301,A*2402,B*3501,B*5701. |
Variant ID. | 3175 |
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Epitope Seq. | {A}ISPRTLNAW |
Variant Seq. | {p}ISPRTLNAW |
Mutations | A/P |
Epitope Location | A-1P |
HXB2 Location | A145P |
Mutation Type | OV: observed variant |
Epitope Subtype | B |
Variant Subtype | B |
Method | Sequence |
Note | Flanking mutation, {p}ISPRTLNAW{V}, was seen for ISW9 from 75 weeks post-infection in patient 3 (P3) who carried HLA alleles A*2402 , A*3201, B*4002, B*5701; from 60 weeks post-infection in P4 who carried HLA alleles A*0101,A*0201,B*5101,B*5701; and from 10 weeks post-infection in P6 who carried HLA alleles A*0301,A*2402,B*3501,B*5701. |
Variant ID. | 3176 |
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Epitope Seq. | {A}ISPRTLNAW |
Variant Seq. | {p}IaPRTLNAW |
Mutations | A/P S/A |
Epitope Location | A-1P S2A |
HXB2 Location | A145P S147A |
Mutation Type | OV: observed variant |
Epitope Subtype | B |
Variant Subtype | B |
Method | Sequence |
Note | Flanking and epitope mutations, {p}IaPRTLNAW{V}, were seen for ISW9 by 274 weeks post-infection in P3 who carried HLA alleles A*2402 , A*3201, B*4002, B*5701. |
Variant ID. | 3177 |
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Epitope Seq. | {A}ISPRTLNAW |
Variant Seq. | {p}ItPRTLNAW |
Mutations | A/P S/T |
Epitope Location | A-1P S2T |
HXB2 Location | A145P S147T |
Mutation Type | OV: observed variant |
Epitope Subtype | B |
Variant Subtype | B |
Method | Sequence |
Note | Flanking and epitope mutations, {p}ItPRTLNAW{V}, were seen for ISW9 by 11 weeks post-infection in P4 who carried HLA alleles A*0101,A*0201,B*5101,B*5701. |
Variant ID. | 3178 |
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Epitope Seq. | {A}ISPRTLNAW |
Variant Seq. | {p}ltPRTLNAW |
Mutations | A/P I/L S/T |
Epitope Location | A-1P I1L S2T |
HXB2 Location | A145P I146L S147T |
Mutation Type | OV: observed variant |
Epitope Subtype | B |
Variant Subtype | B |
Method | Sequence |
Note | Epitope mutation, {A}ItPRTLNAW{V}, was seen for ISW9 by 11 weeks post-infection in P4 who carried HLA alleles A*0101,A*0201,B*5101,B*5701. |
Variant ID. | 3179 |
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Epitope Seq. | ISPRTLNAW |
Variant Seq. | ItPRTLNAW |
Mutations | S/T |
Epitope Location | S2T |
HXB2 Location | S147T |
Mutation Type | OV: observed variant |
Epitope Subtype | B |
Variant Subtype | B |
Method | Sequence |
Note | Flanking and epitope mutations, A|ItPRTLNAW|V, were seen for ISW9 by 316 weeks post-infection in P4 who carried HLA alleles A*0101,A*0201,B*5101,B*5701. |
Variant ID. | 3180 |
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Epitope Seq. | ISPRTLNAW |
Variant Seq. | IlPRTLNAW |
Mutations | S/L |
Epitope Location | S2L |
HXB2 Location | S147L |
Mutation Type | OV: observed variant |
Epitope Subtype | B |
Variant Subtype | B |
Method | Sequence |
Note | Flanking and epitope mutations including IlPRTLNAW, were seen for ISW9 by 45 weeks post-infection in P3 who carried HLA alleles A*2402,A*3201,B*4002,B*5701. |
Norstrom2012 Melissa M. Norström, Marcus Buggert, Johanna Tauriainen, Wendy Hartogensis, Mattia C. Prosperi, Mark A. Wallet, Frederick M. Hecht, Marco Salemi, and Annika C. Karlsson. Combination of Immune and Viral Factors Distinguishes Low-Risk Versus High-Risk HIV-1 Disease Progression in HLA-B*5701 Subjects. J. Virol., 86(18):9802-9816, Sep 2012. PubMed ID: 22761389. Show all entries for this paper.
HXB2 Location | Gag(162-172) | Gag Epitope Map
View variants at this location |
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Epitope |
KAFSPEVIPMF
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Epitope Alignment | |||||||||||||
Variants |
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Epitope Name | KF11 | ||||||||||||||
Species (MHC/HLA) | human(B*57:01) |
Showing all: 4 variant(s).
Variant ID. | 3181 |
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Epitope Seq. | KAFSPEVIPMF |
Variant Seq. | KAFSPEVIPMs |
Mutations | F/S |
Epitope Location | F11S |
HXB2 Location | F171S |
Mutation Type | OV: observed variant |
Epitope Subtype | B |
Variant Subtype | B |
Method | Flow cytometric T-cell cytokine assay |
Note | Epitope mutation, E|KAFSPEVIPMs|S, was seen for KF11 by 104 weeks post-infection in P1 who carried HLA alleles A*0101,A*0301,B*2705,B*5701. |
Variant ID. | 3182 |
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Epitope Seq. | KAFSPEVIPMF |
Variant Seq. | KAFSPEVIPMt |
Mutations | F/T |
Epitope Location | F11T |
HXB2 Location | F171T |
Mutation Type | OV: observed variant |
Epitope Subtype | B |
Variant Subtype | B |
Method | Flow cytometric T-cell cytokine assay |
Note | Epitope mutation, E|KAFSPEVIPMt|S, was seen for KF11 by 168 weeks post-infection in P1 who carried HLA alleles A*0101,A*0301,B*2705,B*5701 and by 377 weeks post-infection in P6 who carried HLA alleles A*0301,A*2402,B*3501,B*5701. |
Variant ID. | 3183 |
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Epitope Seq. | KAFSPEVIPMF |
Variant Seq. | KAFSPEiIPMF |
Mutations | V/I |
Epitope Location | V7I |
HXB2 Location | V167I |
Mutation Type | OV: observed variant |
Epitope Subtype | B |
Variant Subtype | B |
Method | Flow cytometric T-cell cytokine assay |
Note | Epitope mutation, E|KAFSPEiIPMF|S, was seen for KF11 by 168 weeks post-infection in P1 who carried HLA alleles A*0101,A*0301,B*2705,B*5701 and by 301 weeks post-infection in P6 who carried HLA alleles A*0301,A*2402,B*3501,B*5701. |
Variant ID. | 3184 |
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Epitope Seq. | KAFSPEVIPMF |
Variant Seq. | KAsSPEVIPMF |
Mutations | F/S |
Epitope Location | F3S |
HXB2 Location | F163S |
Mutation Type | OV: observed variant |
Epitope Subtype | B |
Variant Subtype | B |
Method | Flow cytometric T-cell cytokine assay |
Note | Epitope mutation, E|KAFSPEVIPMF|S, was seen for KF11 by 301 weeks post-infection in P6 who carried HLA alleles A*0301,A*2402,B*3501,B*5701. |
Norstrom2012 Melissa M. Norström, Marcus Buggert, Johanna Tauriainen, Wendy Hartogensis, Mattia C. Prosperi, Mark A. Wallet, Frederick M. Hecht, Marco Salemi, and Annika C. Karlsson. Combination of Immune and Viral Factors Distinguishes Low-Risk Versus High-Risk HIV-1 Disease Progression in HLA-B*5701 Subjects. J. Virol., 86(18):9802-9816, Sep 2012. PubMed ID: 22761389. Show all entries for this paper.
HXB2 Location | Gag(240-249) | Gag Epitope Map
View variants at this location |
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Epitope |
TSTLQEQIGW
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Epitope Alignment | |||||||||||||||||||||||||
Variants |
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Epitope Name | TW10 | ||||||||||||||||||||||||||
Species (MHC/HLA) | human(B*57:01) |
Showing all: 8 variant(s).
Variant ID. | 3188 |
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Epitope Seq. | TSTLQEQIGW |
Variant Seq. | TSTLrEQIGW |
Mutations | Q/R |
Epitope Location | Q5R |
HXB2 Location | Q243R |
Mutation Type | OV: observed variant |
Epitope Subtype | B |
Variant Subtype | B |
Method | Sequence |
Note | Epitope mutation, T|TSTLrEQIGW|M, was seen for TW10 by the first sampling 13 weeks post-infection in P1 who carried HLA alleles A*0101,A*0301,B*2705,B*5701. |
Variant ID. | 3189 |
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Epitope Seq. | TSTLQEQIGW |
Variant Seq. | TSTLQEQIeW |
Mutations | G/E |
Epitope Location | G9E |
HXB2 Location | G247E |
Mutation Type | OV: observed variant |
Epitope Subtype | B |
Variant Subtype | B |
Method | Sequence |
Note | Epitope mutation, T|TSTLQEQIeW|M, was seen for TW10 by the first sampling 13 weeks post-infection in P1 who carried HLA alleles A*0101,A*0301,B*2705,B*5701 and at 13 weeks post-infection in P5 who carried HLA alleles A*0101,A*0101,B*0801,B*5701. |
Variant ID. | 3190 |
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Epitope Seq. | TSTLQEQIGW |
Variant Seq. | TSnLQEQIGW |
Mutations | T/N |
Epitope Location | T3N |
HXB2 Location | T241N |
Mutation Type | OV: observed variant |
Epitope Subtype | B |
Variant Subtype | B |
Method | Sequence |
Note | Most common epitope mutation, T|TSnLQEQIGW|M, was seen for TW10 by the first sampling 13 weeks post-infection in P1 who carried HLA alleles A*0101,A*0301,B*2705,B*5701; by 18 weeks post-infection in P2 who carried HLA alleles A*0101,A*0301,B*2705,B*5701; by 13 weeks post-infection in P3 who carried HLA alleles A*2402,A*3201,B*4002,B*5701; by 11 weeks post-infection in P4 who carried HLA alleles A*0101,A*0201,B*5101,B*5701 and by 10 weeks post-infection in P6 who carried HLA alleles A*0301,A*2402,B*3501,B*5701. |
Variant ID. | 3192 |
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Epitope Seq. | TSTLQEQIGW |
Variant Seq. | TSsLQEQIGW |
Mutations | T/S |
Epitope Location | T3S |
HXB2 Location | T241S |
Mutation Type | OV: observed variant |
Epitope Subtype | B |
Variant Subtype | B |
Method | Sequence |
Note | Epitope mutation, T|TSsLQEQIGW|M, was seen for TW10 by the first sampling 18 weeks post-infection in P2 who carried HLA alleles A*0101,A*0301,B*2705,B*570. |
Variant ID. | 3193 |
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Epitope Seq. | TSTLQEQIGW |
Variant Seq. | TSnLQEQIrW |
Mutations | T/N G/R |
Epitope Location | T3N G9R |
HXB2 Location | T241N G247R |
Mutation Type | OV: observed variant |
Epitope Subtype | B |
Variant Subtype | B |
Method | Sequence |
Note | Most common epitope mutation, T|TSnLQEQIrW|M, was seen for TW10 by 109 weeks post-infection in P2 who carried HLA alleles A*0101,A*0301,B*2705,B*5701. |
Variant ID. | 3194 |
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Epitope Seq. | TSTLQEQIGW |
Variant Seq. | TSnLQEQIaW |
Mutations | T/N G/A |
Epitope Location | T3N G9A |
HXB2 Location | T241N G247A |
Mutation Type | OV: observed variant |
Epitope Subtype | B |
Variant Subtype | B |
Method | Sequence |
Note | Most common epitope mutation, T|TSnLQEQIaW|M, was seen for TW10 by 45 weeks post-infection in P3 who carried HLA alleles A*2402,A*3201,B*4002,B*5701; by 11 weeks post-infection in P4 who carried the HLA alleles A*0101,A*0201,B*5101,B*5701; and by 144 weeks post-infection in P5 who carried the HLA alleles A*0101,A*0101,B*0801,B*5701. |
Variant ID. | 3195 |
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Epitope Seq. | TSTLQEQIGW |
Variant Seq. | TSnLQEQItW |
Mutations | T/N G/R |
Epitope Location | T3N G9R |
HXB2 Location | T241N G247R |
Mutation Type | OV: observed variant |
Epitope Subtype | B |
Variant Subtype | B |
Method | Sequence |
Note | Most common epitope mutation, T|TSnLQEQIrW|M, was seen for TW10 by 195 weeks post-infection in P2 who carried HLA alleles A*0101,A*0301,B*2705,B*5701. |
Variant ID. | 3196 |
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Epitope Seq. | TSTLQEQIGW |
Variant Seq. | TSTLQEQIaW |
Mutations | G/A |
Epitope Location | G9A |
HXB2 Location | G247A |
Mutation Type | OV: observed variant |
Epitope Subtype | B |
Variant Subtype | B |
Method | Sequence |
Note | Most common epitope mutation, T|TSTLQEQIaW|M, was seen for TW10 by 13 weeks post-infection in P3 who carried HLA alleles A*2402,A*3201,B*4002,B*5701. |
Norstrom2012 Melissa M. Norström, Marcus Buggert, Johanna Tauriainen, Wendy Hartogensis, Mattia C. Prosperi, Mark A. Wallet, Frederick M. Hecht, Marco Salemi, and Annika C. Karlsson. Combination of Immune and Viral Factors Distinguishes Low-Risk Versus High-Risk HIV-1 Disease Progression in HLA-B*5701 Subjects. J. Virol., 86(18):9802-9816, Sep 2012. PubMed ID: 22761389. Show all entries for this paper.
HXB2 Location | Gag(308-316) | Gag Epitope Map
View variants at this location |
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Epitope |
QASQEVKNW
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Epitope Alignment | ||||||||||
Variants |
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Epitope Name | QW9 | |||||||||||
Species (MHC/HLA) | human(B*57:01) |
Showing all: 3 variant(s).
Variant ID. | 3185 |
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Epitope Seq. | QASQEVKNW |
Variant Seq. | QASQdVKNW |
Mutations | E/D |
Epitope Location | E5D |
HXB2 Location | E311D |
Mutation Type | OV: observed variant |
Epitope Subtype | B |
Variant Subtype | B |
Method | Flow cytometric T-cell cytokine assay |
Note | Epitope mutation, E|QASQdVKNW|M, was seen for QW9 by the first sampling 13 weeks post-infection in P1 who carried HLA alleles A*0101,A*0301,B*2705,B*5701; and by 75 weeks post-infection in P3 who carried HLA alleles A*2402,A*3201,B*4002,B*5701. |
Variant ID. | 3186 |
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Epitope Seq. | QASQEVKNW |
Variant Seq. | QASQtVKNW |
Mutations | E/T |
Epitope Location | E5T |
HXB2 Location | E311T |
Mutation Type | OV: observed variant |
Epitope Subtype | B |
Variant Subtype | B |
Method | Flow cytometric T-cell cytokine assay |
Note | Epitope mutation E312T, E|QASQtVKNW|M, was seen for QW9 by the first sampling 18 weeks post-infection in P2 who carried HLA alleles A*0101,A*2402,B*4002,B*5701. |
Variant ID. | 3187 |
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Epitope Seq. | QASQEVKNW |
Variant Seq. | QASkEVKNW |
Mutations | Q/K |
Epitope Location | Q4K |
HXB2 Location | Q310K |
Mutation Type | OV: observed variant |
Epitope Subtype | B |
Variant Subtype | B |
Method | Flow cytometric T-cell cytokine assay |
Note | Minor (4.5%) epitope variation E312K, E|QASkEVKNW|M, was seen for QW9 at 60 weeks post-infection in P4 who carried HLA alleles A*0101,A*0201,B*5101,B*5701. |
Norstrom2012 Melissa M. Norström, Marcus Buggert, Johanna Tauriainen, Wendy Hartogensis, Mattia C. Prosperi, Mark A. Wallet, Frederick M. Hecht, Marco Salemi, and Annika C. Karlsson. Combination of Immune and Viral Factors Distinguishes Low-Risk Versus High-Risk HIV-1 Disease Progression in HLA-B*5701 Subjects. J. Virol., 86(18):9802-9816, Sep 2012. PubMed ID: 22761389. Show all entries for this paper.