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: 70 |
| 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: 37, no: 6 |
| NetGPI | no | yes: 0, no: 43 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005929 | cilium | 4 | 44 |
| GO:0042995 | cell projection | 2 | 44 |
| GO:0043226 | organelle | 2 | 44 |
| GO:0043227 | membrane-bounded organelle | 3 | 44 |
| GO:0110165 | cellular anatomical entity | 1 | 44 |
| GO:0120025 | plasma membrane bounded cell projection | 3 | 44 |
| GO:0016020 | membrane | 2 | 8 |
Related structures:
AlphaFold database: E8NHP8
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 215 | 217 | PF00675 | 0.475 |
| CLV_NRD_NRD_1 | 230 | 232 | PF00675 | 0.327 |
| CLV_NRD_NRD_1 | 50 | 52 | PF00675 | 0.479 |
| CLV_PCSK_KEX2_1 | 215 | 217 | PF00082 | 0.279 |
| CLV_PCSK_SKI1_1 | 107 | 111 | PF00082 | 0.260 |
| CLV_PCSK_SKI1_1 | 15 | 19 | PF00082 | 0.658 |
| CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.446 |
| CLV_PCSK_SKI1_1 | 183 | 187 | PF00082 | 0.309 |
| CLV_PCSK_SKI1_1 | 51 | 55 | PF00082 | 0.402 |
| DEG_APCC_DBOX_1 | 14 | 22 | PF00400 | 0.608 |
| DOC_CDC14_PxL_1 | 94 | 102 | PF14671 | 0.257 |
| DOC_CYCLIN_yClb5_NLxxxL_5 | 190 | 199 | PF00134 | 0.269 |
| DOC_CYCLIN_yClb5_NLxxxL_5 | 238 | 247 | PF00134 | 0.392 |
| DOC_CYCLIN_yCln2_LP_2 | 28 | 31 | PF00134 | 0.370 |
| DOC_MAPK_gen_1 | 13 | 21 | PF00069 | 0.618 |
| DOC_MAPK_gen_1 | 231 | 238 | PF00069 | 0.284 |
| DOC_MAPK_MEF2A_6 | 15 | 23 | PF00069 | 0.415 |
| DOC_PP2B_LxvP_1 | 27 | 30 | PF13499 | 0.601 |
| DOC_USP7_MATH_1 | 178 | 182 | PF00917 | 0.448 |
| DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.503 |
| DOC_USP7_MATH_1 | 293 | 297 | PF00917 | 0.478 |
| DOC_USP7_MATH_2 | 248 | 254 | PF00917 | 0.307 |
| DOC_USP7_UBL2_3 | 120 | 124 | PF12436 | 0.340 |
| DOC_WW_Pin1_4 | 34 | 39 | PF00397 | 0.499 |
| LIG_14-3-3_CanoR_1 | 183 | 188 | PF00244 | 0.452 |
| LIG_14-3-3_CanoR_1 | 231 | 238 | PF00244 | 0.465 |
| LIG_APCC_ABBA_1 | 85 | 90 | PF00400 | 0.285 |
| LIG_BIR_III_2 | 59 | 63 | PF00653 | 0.503 |
| LIG_BRCT_BRCA1_1 | 276 | 280 | PF00533 | 0.501 |
| LIG_BRCT_BRCA1_1 | 68 | 72 | PF00533 | 0.541 |
| LIG_FHA_1 | 146 | 152 | PF00498 | 0.414 |
| LIG_FHA_1 | 170 | 176 | PF00498 | 0.320 |
| LIG_FHA_1 | 194 | 200 | PF00498 | 0.351 |
| LIG_FHA_1 | 218 | 224 | PF00498 | 0.378 |
| LIG_FHA_1 | 22 | 28 | PF00498 | 0.546 |
| LIG_FHA_1 | 242 | 248 | PF00498 | 0.408 |
| LIG_FHA_2 | 133 | 139 | PF00498 | 0.405 |
| LIG_FHA_2 | 172 | 178 | PF00498 | 0.531 |
| LIG_FHA_2 | 235 | 241 | PF00498 | 0.472 |
| LIG_GBD_Chelix_1 | 19 | 27 | PF00786 | 0.588 |
| LIG_KLC1_Yacidic_2 | 86 | 90 | PF13176 | 0.267 |
| LIG_LIR_Gen_1 | 138 | 147 | PF02991 | 0.323 |
| LIG_LIR_Gen_1 | 154 | 161 | PF02991 | 0.289 |
| LIG_LIR_Gen_1 | 177 | 185 | PF02991 | 0.457 |
| LIG_LIR_Gen_1 | 186 | 195 | PF02991 | 0.412 |
| LIG_LIR_Gen_1 | 40 | 48 | PF02991 | 0.502 |
| LIG_LIR_Nem_3 | 130 | 134 | PF02991 | 0.308 |
| LIG_LIR_Nem_3 | 138 | 142 | PF02991 | 0.289 |
| LIG_LIR_Nem_3 | 177 | 182 | PF02991 | 0.322 |
| LIG_LIR_Nem_3 | 186 | 190 | PF02991 | 0.373 |
| LIG_LIR_Nem_3 | 226 | 230 | PF02991 | 0.417 |
| LIG_LIR_Nem_3 | 36 | 42 | PF02991 | 0.531 |
| LIG_Pex14_1 | 163 | 167 | PF04695 | 0.265 |
| LIG_Pex14_2 | 53 | 57 | PF04695 | 0.324 |
| LIG_SH2_CRK | 42 | 46 | PF00017 | 0.408 |
| LIG_SH2_GRB2like | 143 | 146 | PF00017 | 0.359 |
| LIG_SH2_NCK_1 | 42 | 46 | PF00017 | 0.328 |
| LIG_SH2_PTP2 | 108 | 111 | PF00017 | 0.242 |
| LIG_SH2_PTP2 | 139 | 142 | PF00017 | 0.233 |
| LIG_SH2_STAP1 | 143 | 147 | PF00017 | 0.355 |
| LIG_SH2_STAT5 | 108 | 111 | PF00017 | 0.271 |
| LIG_SH2_STAT5 | 139 | 142 | PF00017 | 0.398 |
| LIG_SH2_STAT5 | 77 | 80 | PF00017 | 0.458 |
| LIG_SH2_STAT5 | 88 | 91 | PF00017 | 0.595 |
| LIG_SH3_3 | 92 | 98 | PF00018 | 0.542 |
| LIG_SUMO_SIM_par_1 | 19 | 24 | PF11976 | 0.487 |
| LIG_TYR_ITIM | 137 | 142 | PF00017 | 0.246 |
| LIG_TYR_ITSM | 38 | 45 | PF00017 | 0.320 |
| MOD_CK1_1 | 101 | 107 | PF00069 | 0.342 |
| MOD_CK1_1 | 130 | 136 | PF00069 | 0.353 |
| MOD_CK1_1 | 141 | 147 | PF00069 | 0.363 |
| MOD_CK1_1 | 202 | 208 | PF00069 | 0.421 |
| MOD_CK1_1 | 234 | 240 | PF00069 | 0.429 |
| MOD_CK1_1 | 253 | 259 | PF00069 | 0.509 |
| MOD_CK1_1 | 37 | 43 | PF00069 | 0.526 |
| MOD_CK2_1 | 132 | 138 | PF00069 | 0.266 |
| MOD_CK2_1 | 171 | 177 | PF00069 | 0.521 |
| MOD_CK2_1 | 234 | 240 | PF00069 | 0.301 |
| MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.468 |
| MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.452 |
| MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.486 |
| MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.463 |
| MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.472 |
| MOD_GSK3_1 | 110 | 117 | PF00069 | 0.427 |
| MOD_GSK3_1 | 119 | 126 | PF00069 | 0.483 |
| MOD_GSK3_1 | 141 | 148 | PF00069 | 0.373 |
| MOD_GSK3_1 | 195 | 202 | PF00069 | 0.401 |
| MOD_GSK3_1 | 219 | 226 | PF00069 | 0.365 |
| MOD_GSK3_1 | 232 | 239 | PF00069 | 0.400 |
| MOD_GSK3_1 | 270 | 277 | PF00069 | 0.422 |
| MOD_N-GLC_1 | 193 | 198 | PF02516 | 0.373 |
| MOD_N-GLC_1 | 241 | 246 | PF02516 | 0.380 |
| MOD_N-GLC_2 | 266 | 268 | PF02516 | 0.291 |
| MOD_N-GLC_2 | 299 | 301 | PF02516 | 0.580 |
| MOD_NEK2_1 | 110 | 115 | PF00069 | 0.404 |
| MOD_NEK2_1 | 123 | 128 | PF00069 | 0.336 |
| MOD_NEK2_1 | 147 | 152 | PF00069 | 0.385 |
| MOD_NEK2_1 | 171 | 176 | PF00069 | 0.317 |
| MOD_NEK2_1 | 195 | 200 | PF00069 | 0.343 |
| MOD_NEK2_1 | 219 | 224 | PF00069 | 0.376 |
| MOD_NEK2_1 | 243 | 248 | PF00069 | 0.384 |
| MOD_NEK2_2 | 119 | 124 | PF00069 | 0.354 |
| MOD_NEK2_2 | 178 | 183 | PF00069 | 0.245 |
| MOD_PK_1 | 232 | 238 | PF00069 | 0.273 |
| MOD_PK_1 | 66 | 72 | PF00069 | 0.294 |
| MOD_PKA_1 | 231 | 237 | PF00069 | 0.286 |
| MOD_PKA_2 | 217 | 223 | PF00069 | 0.440 |
| MOD_Plk_4 | 138 | 144 | PF00069 | 0.354 |
| MOD_Plk_4 | 253 | 259 | PF00069 | 0.403 |
| MOD_Plk_4 | 286 | 292 | PF00069 | 0.487 |
| MOD_ProDKin_1 | 34 | 40 | PF00069 | 0.499 |
| TRG_DiLeu_BaEn_1 | 14 | 19 | PF01217 | 0.364 |
| TRG_DiLeu_BaLyEn_6 | 59 | 64 | PF01217 | 0.317 |
| TRG_ENDOCYTIC_2 | 108 | 111 | PF00928 | 0.395 |
| TRG_ENDOCYTIC_2 | 139 | 142 | PF00928 | 0.400 |
| TRG_ENDOCYTIC_2 | 42 | 45 | PF00928 | 0.414 |
| TRG_ER_diArg_1 | 215 | 218 | PF00400 | 0.248 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P227 | Leptomonas seymouri | 31% | 97% |
| A0A0N0P276 | Leptomonas seymouri | 29% | 98% |
| A0A0N0P2L4 | Leptomonas seymouri | 30% | 100% |
| A0A0N0P4M2 | Leptomonas seymouri | 25% | 100% |
| A0A0N1HY53 | Leptomonas seymouri | 35% | 100% |
| A0A0S4IIK7 | Bodo saltans | 26% | 73% |
| A0A0S4IN83 | Bodo saltans | 31% | 100% |
| A0A0S4IQP4 | Bodo saltans | 35% | 77% |
| A0A0S4IR61 | Bodo saltans | 27% | 75% |
| A0A0S4IVN7 | Bodo saltans | 34% | 79% |
| A0A0S4IZC7 | Bodo saltans | 31% | 74% |
| A0A0S4J2R4 | Bodo saltans | 30% | 90% |
| A0A0S4J353 | Bodo saltans | 24% | 100% |
| A0A0S4J3T7 | Bodo saltans | 33% | 67% |
| A0A0S4J805 | Bodo saltans | 29% | 100% |
| A0A0S4JEK1 | Bodo saltans | 28% | 74% |
| A0A0S4JEZ2 | Bodo saltans | 29% | 95% |
| A0A0S4JS12 | Bodo saltans | 28% | 67% |
| A0A0S4KHE4 | Bodo saltans | 34% | 82% |
| A0A1X0NKN8 | Trypanosomatidae | 27% | 100% |
| A0A3Q8I9A6 | Leishmania donovani | 32% | 78% |
| A0A3Q8I9D0 | Leishmania donovani | 36% | 100% |
| A0A3Q8IFC2 | Leishmania donovani | 32% | 69% |
| A0A3Q8IIJ9 | Leishmania donovani | 87% | 100% |
| A0A3S5H6D6 | Leishmania donovani | 27% | 100% |
| A0A3S7WPB2 | Leishmania donovani | 26% | 100% |
| A0A3S7X4J4 | Leishmania donovani | 86% | 100% |
| A4H4G6 | Leishmania braziliensis | 27% | 100% |
| A4H5P0 | Leishmania braziliensis | 29% | 100% |
| A4HBX3 | Leishmania braziliensis | 36% | 67% |
| A4HJC8 | Leishmania braziliensis | 70% | 100% |
| A4HJX1 | Leishmania braziliensis | 32% | 100% |
| A4HTX9 | Leishmania infantum | 27% | 100% |
| A4HVB0 | Leishmania infantum | 32% | 75% |
| A4I6S2 | Leishmania infantum | 30% | 69% |
| A4I6S4 | Leishmania infantum | 87% | 100% |
| E8NHG5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 68% |
| E9ACQ0 | Leishmania major | 26% | 100% |
| E9AG65 | Leishmania infantum | 26% | 100% |
| E9AGG5 | Leishmania infantum | 31% | 73% |
| E9AGH0 | Leishmania infantum | 35% | 80% |
| E9AKM8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
| E9AMQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
| E9AP02 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 89% |
| E9AP03 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 77% |
| E9AP07 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 83% |
| E9AP08 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 72% |
| E9B1U3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 67% |
| E9B1U4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 89% |
| E9B1U5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 72% |
| E9B1U6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 99% | 100% |
| F4HTV6 | Arabidopsis thaliana | 25% | 100% |
| P58822 | Phaseolus vulgaris | 25% | 89% |
| P58823 | Phaseolus vulgaris | 25% | 89% |
| Q25331 | Leishmania major | 31% | 100% |
| Q4PSE6 | Arabidopsis thaliana | 26% | 70% |
| Q4Q6B6 | Leishmania major | 88% | 100% |
| Q4Q6B7 | Leishmania major | 88% | 100% |
| Q4QC79 | Leishmania major | 33% | 66% |
| Q4QGJ4 | Leishmania major | 31% | 100% |
| Q4QGJ7 | Leishmania major | 31% | 100% |
| Q4QGK6 | Leishmania major | 31% | 100% |
| Q4QGL4 | Leishmania major | 35% | 100% |
| Q4QHW6 | Leishmania major | 27% | 100% |
| Q8GT95 | Oryza sativa subsp. japonica | 26% | 91% |
| Q8W3M4 | Arabidopsis thaliana | 24% | 75% |
| Q9LH52 | Arabidopsis thaliana | 24% | 93% |
| Q9M5J8 | Arabidopsis thaliana | 28% | 92% |
| Q9M5J9 | Arabidopsis thaliana | 26% | 92% |