Publication identifier(s): 8702946
A surface coat protein involved in immune evasion in Leishmaniids. Extremely fast evolving, almost completely disordered mucin-like protein. . Localization: Cell surface (experimental)
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 45 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | yes | yes: 31, no: 8 |
NetGPI | no | yes: 0, no: 39 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 40 |
GO:0042995 | cell projection | 2 | 40 |
GO:0043226 | organelle | 2 | 40 |
GO:0043227 | membrane-bounded organelle | 3 | 40 |
GO:0110165 | cellular anatomical entity | 1 | 40 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 40 |
GO:0016020 | membrane | 2 | 4 |
Related structures:
AlphaFold database: Q4Q6B7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 237 | 241 | PF00656 | 0.289 |
CLV_NRD_NRD_1 | 230 | 232 | PF00675 | 0.341 |
CLV_NRD_NRD_1 | 50 | 52 | PF00675 | 0.336 |
CLV_PCSK_SKI1_1 | 107 | 111 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 15 | 19 | PF00082 | 0.576 |
CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 183 | 187 | PF00082 | 0.336 |
CLV_PCSK_SKI1_1 | 51 | 55 | PF00082 | 0.501 |
DEG_APCC_DBOX_1 | 14 | 22 | PF00400 | 0.632 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 190 | 199 | PF00134 | 0.454 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 238 | 247 | PF00134 | 0.383 |
DOC_MAPK_gen_1 | 13 | 21 | PF00069 | 0.613 |
DOC_MAPK_gen_1 | 231 | 238 | PF00069 | 0.309 |
DOC_MAPK_MEF2A_6 | 15 | 23 | PF00069 | 0.542 |
DOC_PP2B_LxvP_1 | 28 | 31 | PF13499 | 0.459 |
DOC_USP7_MATH_1 | 178 | 182 | PF00917 | 0.460 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.415 |
DOC_USP7_MATH_1 | 293 | 297 | PF00917 | 0.487 |
DOC_USP7_MATH_1 | 98 | 102 | PF00917 | 0.524 |
DOC_USP7_MATH_2 | 248 | 254 | PF00917 | 0.338 |
DOC_USP7_UBL2_3 | 120 | 124 | PF12436 | 0.345 |
DOC_USP7_UBL2_3 | 43 | 47 | PF12436 | 0.262 |
DOC_WW_Pin1_4 | 34 | 39 | PF00397 | 0.537 |
LIG_14-3-3_CanoR_1 | 183 | 188 | PF00244 | 0.321 |
LIG_14-3-3_CanoR_1 | 231 | 238 | PF00244 | 0.438 |
LIG_Actin_WH2_2 | 216 | 233 | PF00022 | 0.543 |
LIG_APCC_ABBA_1 | 85 | 90 | PF00400 | 0.298 |
LIG_BIR_III_2 | 59 | 63 | PF00653 | 0.349 |
LIG_BRCT_BRCA1_1 | 276 | 280 | PF00533 | 0.527 |
LIG_BRCT_BRCA1_1 | 68 | 72 | PF00533 | 0.323 |
LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.407 |
LIG_FHA_1 | 146 | 152 | PF00498 | 0.404 |
LIG_FHA_1 | 170 | 176 | PF00498 | 0.332 |
LIG_FHA_1 | 194 | 200 | PF00498 | 0.418 |
LIG_FHA_1 | 218 | 224 | PF00498 | 0.391 |
LIG_FHA_1 | 22 | 28 | PF00498 | 0.568 |
LIG_FHA_1 | 242 | 248 | PF00498 | 0.395 |
LIG_FHA_2 | 133 | 139 | PF00498 | 0.383 |
LIG_FHA_2 | 172 | 178 | PF00498 | 0.544 |
LIG_FHA_2 | 208 | 214 | PF00498 | 0.469 |
LIG_FHA_2 | 235 | 241 | PF00498 | 0.494 |
LIG_GBD_Chelix_1 | 19 | 27 | PF00786 | 0.629 |
LIG_LIR_Gen_1 | 138 | 147 | PF02991 | 0.361 |
LIG_LIR_Gen_1 | 154 | 161 | PF02991 | 0.324 |
LIG_LIR_Gen_1 | 177 | 185 | PF02991 | 0.356 |
LIG_LIR_Gen_1 | 186 | 195 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 130 | 134 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 138 | 142 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 160 | 166 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 177 | 182 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 186 | 190 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 226 | 230 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 36 | 42 | PF02991 | 0.542 |
LIG_NRBOX | 24 | 30 | PF00104 | 0.605 |
LIG_Pex14_1 | 163 | 167 | PF04695 | 0.465 |
LIG_Pex14_2 | 53 | 57 | PF04695 | 0.474 |
LIG_SH2_CRK | 42 | 46 | PF00017 | 0.389 |
LIG_SH2_GRB2like | 143 | 146 | PF00017 | 0.362 |
LIG_SH2_PTP2 | 108 | 111 | PF00017 | 0.248 |
LIG_SH2_PTP2 | 139 | 142 | PF00017 | 0.240 |
LIG_SH2_STAP1 | 143 | 147 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 108 | 111 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 139 | 142 | PF00017 | 0.332 |
LIG_SH2_STAT5 | 88 | 91 | PF00017 | 0.374 |
LIG_SH3_3 | 92 | 98 | PF00018 | 0.395 |
LIG_TYR_ITIM | 137 | 142 | PF00017 | 0.432 |
LIG_TYR_ITSM | 38 | 45 | PF00017 | 0.318 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.317 |
MOD_CK1_1 | 130 | 136 | PF00069 | 0.374 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.358 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.474 |
MOD_CK1_1 | 234 | 240 | PF00069 | 0.392 |
MOD_CK1_1 | 37 | 43 | PF00069 | 0.541 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.453 |
MOD_CK2_1 | 132 | 138 | PF00069 | 0.425 |
MOD_CK2_1 | 171 | 177 | PF00069 | 0.526 |
MOD_CK2_1 | 207 | 213 | PF00069 | 0.472 |
MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.410 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.441 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.484 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.354 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.412 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.394 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.439 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.444 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.323 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.412 |
MOD_N-GLC_1 | 114 | 119 | PF02516 | 0.450 |
MOD_N-GLC_1 | 193 | 198 | PF02516 | 0.366 |
MOD_N-GLC_1 | 241 | 246 | PF02516 | 0.421 |
MOD_N-GLC_2 | 266 | 268 | PF02516 | 0.481 |
MOD_N-GLC_2 | 299 | 301 | PF02516 | 0.496 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.365 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.308 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.332 |
MOD_NEK2_1 | 171 | 176 | PF00069 | 0.352 |
MOD_NEK2_1 | 195 | 200 | PF00069 | 0.374 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.361 |
MOD_NEK2_2 | 119 | 124 | PF00069 | 0.572 |
MOD_NEK2_2 | 178 | 183 | PF00069 | 0.461 |
MOD_PIKK_1 | 37 | 43 | PF00454 | 0.474 |
MOD_PK_1 | 232 | 238 | PF00069 | 0.288 |
MOD_PK_1 | 66 | 72 | PF00069 | 0.300 |
MOD_PKA_1 | 231 | 237 | PF00069 | 0.302 |
MOD_PKA_2 | 217 | 223 | PF00069 | 0.551 |
MOD_Plk_1 | 114 | 120 | PF00069 | 0.398 |
MOD_Plk_1 | 286 | 292 | PF00069 | 0.450 |
MOD_Plk_4 | 207 | 213 | PF00069 | 0.486 |
MOD_Plk_4 | 276 | 282 | PF00069 | 0.421 |
MOD_Plk_4 | 286 | 292 | PF00069 | 0.361 |
MOD_ProDKin_1 | 34 | 40 | PF00069 | 0.537 |
TRG_DiLeu_BaLyEn_6 | 59 | 64 | PF01217 | 0.332 |
TRG_ENDOCYTIC_2 | 108 | 111 | PF00928 | 0.485 |
TRG_ENDOCYTIC_2 | 139 | 142 | PF00928 | 0.369 |
TRG_ENDOCYTIC_2 | 42 | 45 | PF00928 | 0.378 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P227 | Leptomonas seymouri | 31% | 96% |
A0A0N0P276 | Leptomonas seymouri | 27% | 98% |
A0A0N0P2L4 | Leptomonas seymouri | 28% | 100% |
A0A0N0P4M2 | Leptomonas seymouri | 32% | 100% |
A0A0N1HY53 | Leptomonas seymouri | 33% | 100% |
A0A0S4IIK7 | Bodo saltans | 27% | 73% |
A0A0S4IQP4 | Bodo saltans | 35% | 77% |
A0A0S4IVN7 | Bodo saltans | 34% | 79% |
A0A0S4IZC7 | Bodo saltans | 27% | 73% |
A0A0S4J353 | Bodo saltans | 24% | 100% |
A0A0S4J3T7 | Bodo saltans | 31% | 67% |
A0A0S4JCG7 | Bodo saltans | 32% | 80% |
A0A0S4JEK1 | Bodo saltans | 28% | 74% |
A0A0S4JHM1 | Bodo saltans | 28% | 93% |
A0A0S4JMF9 | Bodo saltans | 31% | 76% |
A0A0S4JMG0 | Bodo saltans | 30% | 87% |
A0A0S4JP32 | Bodo saltans | 28% | 100% |
A0A0S4JS11 | Bodo saltans | 32% | 94% |
A0A0S4KFY6 | Bodo saltans | 33% | 91% |
A0A0S4KHE4 | Bodo saltans | 30% | 82% |
A0A0S4KMV2 | Bodo saltans | 29% | 77% |
A0A1X0NKN8 | Trypanosomatidae | 27% | 100% |
A0A3Q8I9A6 | Leishmania donovani | 34% | 78% |
A0A3Q8I9D0 | Leishmania donovani | 36% | 100% |
A0A3Q8IFC2 | Leishmania donovani | 32% | 69% |
A0A3Q8IIJ9 | Leishmania donovani | 91% | 100% |
A0A3S5H6D6 | Leishmania donovani | 27% | 100% |
A0A3S7WPB2 | Leishmania donovani | 26% | 100% |
A0A3S7X4J4 | Leishmania donovani | 90% | 100% |
A4H4D2 | Leishmania braziliensis | 24% | 100% |
A4H4G6 | Leishmania braziliensis | 29% | 100% |
A4H5P0 | Leishmania braziliensis | 29% | 100% |
A4HBX3 | Leishmania braziliensis | 36% | 67% |
A4HJC8 | Leishmania braziliensis | 69% | 100% |
A4HJX1 | Leishmania braziliensis | 34% | 69% |
A4HTX9 | Leishmania infantum | 27% | 100% |
A4HVB0 | Leishmania infantum | 34% | 75% |
A4I6S2 | Leishmania infantum | 32% | 69% |
A4I6S4 | Leishmania infantum | 91% | 100% |
E8NHG5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 68% |
E8NHP8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
E9ACQ0 | Leishmania major | 26% | 100% |
E9AG65 | Leishmania infantum | 26% | 100% |
E9AGG5 | Leishmania infantum | 33% | 72% |
E9AGH0 | Leishmania infantum | 35% | 80% |
E9AKM8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9AMQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9AP02 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 89% |
E9AP03 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 77% |
E9AP07 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 82% |
E9AP08 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 72% |
E9B1U3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 66% |
E9B1U4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 88% |
E9B1U5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 72% |
E9B1U6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
P35334 | Phaseolus vulgaris | 24% | 88% |
Q00874 | Arabidopsis thaliana | 26% | 81% |
Q25331 | Leishmania major | 30% | 100% |
Q4PSE6 | Arabidopsis thaliana | 26% | 70% |
Q4Q6B6 | Leishmania major | 100% | 100% |
Q4QC79 | Leishmania major | 38% | 66% |
Q4QGJ4 | Leishmania major | 29% | 78% |
Q4QGJ7 | Leishmania major | 29% | 81% |
Q4QGK6 | Leishmania major | 29% | 78% |
Q4QGL4 | Leishmania major | 33% | 76% |
Q4QHW6 | Leishmania major | 28% | 100% |
Q6NQP4 | Arabidopsis thaliana | 29% | 100% |
Q8GT95 | Oryza sativa subsp. japonica | 26% | 91% |
Q8W3M4 | Arabidopsis thaliana | 26% | 75% |
Q9FPJ5 | Arabidopsis thaliana | 30% | 100% |
Q9LH52 | Arabidopsis thaliana | 24% | 93% |
Q9M5J8 | Arabidopsis thaliana | 29% | 92% |
Q9M5J9 | Arabidopsis thaliana | 27% | 92% |