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. | yes | yes: 50 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 7 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | yes | yes: 24, no: 1 |
NetGPI | no | yes: 0, no: 25 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 26 |
GO:0042995 | cell projection | 2 | 26 |
GO:0043226 | organelle | 2 | 26 |
GO:0043227 | membrane-bounded organelle | 3 | 26 |
GO:0110165 | cellular anatomical entity | 1 | 26 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 26 |
GO:0016020 | membrane | 2 | 6 |
Related structures:
AlphaFold database: A4I6S2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 224 | 226 | PF00675 | 0.351 |
CLV_NRD_NRD_1 | 363 | 365 | PF00675 | 0.536 |
CLV_NRD_NRD_1 | 374 | 376 | PF00675 | 0.536 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.453 |
CLV_PCSK_KEX2_1 | 224 | 226 | PF00082 | 0.335 |
CLV_PCSK_KEX2_1 | 363 | 365 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 374 | 376 | PF00082 | 0.536 |
CLV_PCSK_KEX2_1 | 6 | 8 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 176 | 180 | PF00082 | 0.386 |
CLV_PCSK_SKI1_1 | 7 | 11 | PF00082 | 0.574 |
DEG_APCC_DBOX_1 | 405 | 413 | PF00400 | 0.535 |
DEG_APCC_DBOX_1 | 6 | 14 | PF00400 | 0.504 |
DEG_SCF_FBW7_1 | 323 | 328 | PF00400 | 0.553 |
DEG_SPOP_SBC_1 | 291 | 295 | PF00917 | 0.603 |
DEG_SPOP_SBC_1 | 299 | 303 | PF00917 | 0.588 |
DOC_MAPK_gen_1 | 147 | 156 | PF00069 | 0.317 |
DOC_MAPK_gen_1 | 371 | 379 | PF00069 | 0.538 |
DOC_MAPK_gen_1 | 6 | 13 | PF00069 | 0.460 |
DOC_PP1_RVXF_1 | 222 | 229 | PF00149 | 0.308 |
DOC_PP2B_LxvP_1 | 22 | 25 | PF13499 | 0.523 |
DOC_USP7_MATH_1 | 102 | 106 | PF00917 | 0.396 |
DOC_USP7_MATH_1 | 192 | 196 | PF00917 | 0.342 |
DOC_USP7_MATH_1 | 298 | 302 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 323 | 327 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 348 | 352 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.335 |
DOC_USP7_MATH_1 | 74 | 78 | PF00917 | 0.301 |
DOC_WW_Pin1_4 | 265 | 270 | PF00397 | 0.373 |
DOC_WW_Pin1_4 | 292 | 297 | PF00397 | 0.580 |
DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.527 |
DOC_WW_Pin1_4 | 321 | 326 | PF00397 | 0.557 |
DOC_WW_Pin1_4 | 346 | 351 | PF00397 | 0.568 |
LIG_14-3-3_CanoR_1 | 176 | 181 | PF00244 | 0.291 |
LIG_14-3-3_CanoR_1 | 61 | 66 | PF00244 | 0.370 |
LIG_BRCT_BRCA1_1 | 173 | 177 | PF00533 | 0.324 |
LIG_Clathr_ClatBox_1 | 122 | 126 | PF01394 | 0.302 |
LIG_deltaCOP1_diTrp_1 | 263 | 272 | PF00928 | 0.368 |
LIG_DLG_GKlike_1 | 243 | 250 | PF00625 | 0.337 |
LIG_FHA_1 | 101 | 107 | PF00498 | 0.408 |
LIG_FHA_1 | 136 | 142 | PF00498 | 0.359 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.314 |
LIG_FHA_1 | 208 | 214 | PF00498 | 0.427 |
LIG_FHA_1 | 268 | 274 | PF00498 | 0.372 |
LIG_FHA_1 | 412 | 418 | PF00498 | 0.548 |
LIG_FHA_1 | 62 | 68 | PF00498 | 0.430 |
LIG_FHA_2 | 108 | 114 | PF00498 | 0.579 |
LIG_FHA_2 | 210 | 216 | PF00498 | 0.467 |
LIG_FHA_2 | 292 | 298 | PF00498 | 0.585 |
LIG_FHA_2 | 317 | 323 | PF00498 | 0.570 |
LIG_FHA_2 | 342 | 348 | PF00498 | 0.562 |
LIG_LIR_Gen_1 | 117 | 128 | PF02991 | 0.361 |
LIG_LIR_Gen_1 | 143 | 151 | PF02991 | 0.392 |
LIG_LIR_Gen_1 | 168 | 177 | PF02991 | 0.358 |
LIG_LIR_Gen_1 | 215 | 223 | PF02991 | 0.399 |
LIG_LIR_Gen_1 | 240 | 247 | PF02991 | 0.460 |
LIG_LIR_Gen_1 | 33 | 43 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 117 | 123 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 143 | 148 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 174 | 180 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 183 | 189 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 270 | 275 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 33 | 38 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 430 | 435 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 87 | 91 | PF02991 | 0.413 |
LIG_MYND_3 | 244 | 248 | PF01753 | 0.349 |
LIG_Pex14_2 | 237 | 241 | PF04695 | 0.317 |
LIG_PTB_Apo_2 | 251 | 258 | PF02174 | 0.306 |
LIG_SH2_CRK | 120 | 124 | PF00017 | 0.363 |
LIG_SH2_CRK | 158 | 162 | PF00017 | 0.317 |
LIG_SH2_NCK_1 | 158 | 162 | PF00017 | 0.317 |
LIG_SH2_STAP1 | 392 | 396 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 158 | 161 | PF00017 | 0.532 |
LIG_SH3_3 | 109 | 115 | PF00018 | 0.403 |
LIG_SH3_3 | 28 | 34 | PF00018 | 0.487 |
LIG_SH3_CIN85_PxpxPR_1 | 401 | 406 | PF14604 | 0.538 |
LIG_SUMO_SIM_par_1 | 378 | 383 | PF11976 | 0.529 |
LIG_TYR_ITIM | 118 | 123 | PF00017 | 0.444 |
LIG_TYR_ITIM | 156 | 161 | PF00017 | 0.348 |
MOD_CK1_1 | 105 | 111 | PF00069 | 0.390 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.490 |
MOD_CK1_1 | 160 | 166 | PF00069 | 0.418 |
MOD_CK1_1 | 168 | 174 | PF00069 | 0.477 |
MOD_CK1_1 | 194 | 200 | PF00069 | 0.500 |
MOD_CK1_1 | 264 | 270 | PF00069 | 0.399 |
MOD_CK1_1 | 302 | 308 | PF00069 | 0.599 |
MOD_CK1_1 | 310 | 316 | PF00069 | 0.660 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.579 |
MOD_CK1_1 | 335 | 341 | PF00069 | 0.558 |
MOD_CK1_1 | 351 | 357 | PF00069 | 0.565 |
MOD_CK2_1 | 107 | 113 | PF00069 | 0.509 |
MOD_CK2_1 | 194 | 200 | PF00069 | 0.460 |
MOD_CK2_1 | 209 | 215 | PF00069 | 0.364 |
MOD_CK2_1 | 291 | 297 | PF00069 | 0.560 |
MOD_CK2_1 | 302 | 308 | PF00069 | 0.559 |
MOD_CK2_1 | 316 | 322 | PF00069 | 0.558 |
MOD_CK2_1 | 327 | 333 | PF00069 | 0.554 |
MOD_CK2_1 | 341 | 347 | PF00069 | 0.551 |
MOD_CK2_1 | 54 | 60 | PF00069 | 0.510 |
MOD_Cter_Amidation | 372 | 375 | PF01082 | 0.531 |
MOD_DYRK1A_RPxSP_1 | 30 | 34 | PF00069 | 0.468 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.390 |
MOD_GlcNHglycan | 302 | 305 | PF01048 | 0.578 |
MOD_GlcNHglycan | 308 | 312 | PF01048 | 0.596 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.536 |
MOD_GlcNHglycan | 333 | 337 | PF01048 | 0.554 |
MOD_GlcNHglycan | 351 | 354 | PF01048 | 0.552 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.361 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.467 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.424 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.477 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.345 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.404 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.600 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.610 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.652 |
MOD_GSK3_1 | 317 | 324 | PF00069 | 0.640 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.567 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.564 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.355 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.394 |
MOD_N-GLC_1 | 96 | 101 | PF02516 | 0.319 |
MOD_N-GLC_2 | 256 | 258 | PF02516 | 0.406 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.364 |
MOD_NEK2_1 | 156 | 161 | PF00069 | 0.336 |
MOD_NEK2_1 | 178 | 183 | PF00069 | 0.294 |
MOD_NEK2_1 | 233 | 238 | PF00069 | 0.444 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.432 |
MOD_PIKK_1 | 204 | 210 | PF00454 | 0.350 |
MOD_PKB_1 | 426 | 434 | PF00069 | 0.499 |
MOD_Plk_1 | 118 | 124 | PF00069 | 0.485 |
MOD_Plk_1 | 215 | 221 | PF00069 | 0.402 |
MOD_Plk_1 | 96 | 102 | PF00069 | 0.327 |
MOD_Plk_4 | 118 | 124 | PF00069 | 0.359 |
MOD_Plk_4 | 261 | 267 | PF00069 | 0.403 |
MOD_Plk_4 | 96 | 102 | PF00069 | 0.364 |
MOD_ProDKin_1 | 265 | 271 | PF00069 | 0.367 |
MOD_ProDKin_1 | 292 | 298 | PF00069 | 0.581 |
MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.519 |
MOD_ProDKin_1 | 321 | 327 | PF00069 | 0.558 |
MOD_ProDKin_1 | 346 | 352 | PF00069 | 0.568 |
TRG_ENDOCYTIC_2 | 120 | 123 | PF00928 | 0.506 |
TRG_ENDOCYTIC_2 | 158 | 161 | PF00928 | 0.380 |
TRG_ENDOCYTIC_2 | 234 | 237 | PF00928 | 0.374 |
TRG_ER_diArg_1 | 223 | 225 | PF00400 | 0.351 |
TRG_ER_diArg_1 | 28 | 31 | PF00400 | 0.468 |
TRG_ER_diArg_1 | 412 | 415 | PF00400 | 0.531 |
TRG_ER_diArg_1 | 425 | 428 | PF00400 | 0.501 |
TRG_ER_diArg_1 | 6 | 8 | PF00400 | 0.462 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I121 | Leptomonas seymouri | 25% | 88% |
A0A3Q8I9A6 | Leishmania donovani | 35% | 100% |
A0A3Q8IIJ9 | Leishmania donovani | 29% | 100% |
A0A3Q8IK15 | Leishmania donovani | 97% | 83% |
A0A3S7X4J4 | Leishmania donovani | 29% | 100% |
A4H4D2 | Leishmania braziliensis | 28% | 100% |
A4HJC8 | Leishmania braziliensis | 30% | 100% |
A4HVB0 | Leishmania infantum | 35% | 100% |
A4I6S4 | Leishmania infantum | 30% | 100% |
E8NHP8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E8NHQ6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 67% |
E9AGG5 | Leishmania infantum | 35% | 100% |
E9AGH0 | Leishmania infantum | 37% | 100% |
E9AP02 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 42% | 100% |
E9AP03 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 100% |
E9AP07 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 43% | 100% |
E9B1U4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
E9B1U6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
Q4Q6B6 | Leishmania major | 31% | 100% |
Q4Q6B7 | Leishmania major | 32% | 100% |
Q4Q6B8 | Leishmania major | 82% | 83% |
Q4QGJ6 | Leishmania major | 31% | 77% |
Q4QGL4 | Leishmania major | 32% | 100% |
Q4QGL5 | Leishmania major | 33% | 80% |