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: 0 |
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 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 1 |
GO:0042995 | cell projection | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 1 |
Related structures:
AlphaFold database: A4HIG8
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 12 |
GO:0008270 | zinc ion binding | 6 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043169 | cation binding | 3 | 12 |
GO:0046872 | metal ion binding | 4 | 12 |
GO:0046914 | transition metal ion binding | 5 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 254 | 258 | PF00656 | 0.408 |
CLV_C14_Caspase3-7 | 443 | 447 | PF00656 | 0.391 |
CLV_NRD_NRD_1 | 136 | 138 | PF00675 | 0.227 |
CLV_NRD_NRD_1 | 246 | 248 | PF00675 | 0.424 |
CLV_PCSK_KEX2_1 | 119 | 121 | PF00082 | 0.412 |
CLV_PCSK_KEX2_1 | 136 | 138 | PF00082 | 0.243 |
CLV_PCSK_KEX2_1 | 246 | 248 | PF00082 | 0.551 |
CLV_PCSK_PC1ET2_1 | 119 | 121 | PF00082 | 0.412 |
CLV_PCSK_PC7_1 | 115 | 121 | PF00082 | 0.447 |
CLV_PCSK_PC7_1 | 132 | 138 | PF00082 | 0.130 |
CLV_PCSK_SKI1_1 | 247 | 251 | PF00082 | 0.444 |
CLV_PCSK_SKI1_1 | 4 | 8 | PF00082 | 0.441 |
CLV_PCSK_SKI1_1 | 418 | 422 | PF00082 | 0.577 |
DEG_APCC_DBOX_1 | 245 | 253 | PF00400 | 0.433 |
DEG_SCF_TRCP1_1 | 254 | 259 | PF00400 | 0.421 |
DOC_ANK_TNKS_1 | 119 | 126 | PF00023 | 0.415 |
DOC_CYCLIN_yClb1_LxF_4 | 379 | 384 | PF00134 | 0.408 |
DOC_CYCLIN_yCln2_LP_2 | 15 | 21 | PF00134 | 0.258 |
DOC_CYCLIN_yCln2_LP_2 | 376 | 382 | PF00134 | 0.479 |
DOC_MAPK_gen_1 | 353 | 362 | PF00069 | 0.648 |
DOC_MAPK_MEF2A_6 | 170 | 177 | PF00069 | 0.308 |
DOC_PP1_RVXF_1 | 379 | 385 | PF00149 | 0.407 |
DOC_PP2B_LxvP_1 | 376 | 379 | PF13499 | 0.371 |
DOC_USP7_MATH_1 | 538 | 542 | PF00917 | 0.411 |
DOC_USP7_UBL2_3 | 355 | 359 | PF12436 | 0.445 |
LIG_14-3-3_CanoR_1 | 211 | 215 | PF00244 | 0.441 |
LIG_14-3-3_CanoR_1 | 246 | 250 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 296 | 304 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 381 | 385 | PF00244 | 0.371 |
LIG_14-3-3_CanoR_1 | 4 | 12 | PF00244 | 0.302 |
LIG_14-3-3_CanoR_1 | 432 | 438 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 481 | 490 | PF00244 | 0.437 |
LIG_Actin_WH2_2 | 368 | 383 | PF00022 | 0.373 |
LIG_Actin_WH2_2 | 387 | 404 | PF00022 | 0.398 |
LIG_Actin_WH2_2 | 494 | 512 | PF00022 | 0.421 |
LIG_APCC_ABBA_1 | 166 | 171 | PF00400 | 0.388 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.495 |
LIG_BRCT_BRCA1_1 | 130 | 134 | PF00533 | 0.487 |
LIG_BRCT_BRCA1_1 | 444 | 448 | PF00533 | 0.526 |
LIG_FHA_1 | 381 | 387 | PF00498 | 0.431 |
LIG_FHA_1 | 481 | 487 | PF00498 | 0.496 |
LIG_FHA_1 | 5 | 11 | PF00498 | 0.258 |
LIG_FHA_1 | 91 | 97 | PF00498 | 0.256 |
LIG_FHA_2 | 224 | 230 | PF00498 | 0.477 |
LIG_FHA_2 | 287 | 293 | PF00498 | 0.462 |
LIG_KLC1_Yacidic_2 | 70 | 74 | PF13176 | 0.511 |
LIG_LIR_Apic_2 | 463 | 469 | PF02991 | 0.391 |
LIG_LIR_Gen_1 | 217 | 227 | PF02991 | 0.383 |
LIG_LIR_Gen_1 | 228 | 239 | PF02991 | 0.386 |
LIG_LIR_Gen_1 | 70 | 80 | PF02991 | 0.678 |
LIG_LIR_Nem_3 | 217 | 223 | PF02991 | 0.397 |
LIG_LIR_Nem_3 | 228 | 234 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 314 | 319 | PF02991 | 0.568 |
LIG_LIR_Nem_3 | 419 | 424 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 445 | 451 | PF02991 | 0.469 |
LIG_PDZ_Class_2 | 541 | 546 | PF00595 | 0.367 |
LIG_SH2_NCK_1 | 220 | 224 | PF00017 | 0.389 |
LIG_SH2_SRC | 64 | 67 | PF00017 | 0.495 |
LIG_SH2_STAP1 | 216 | 220 | PF00017 | 0.527 |
LIG_SH2_STAP1 | 482 | 486 | PF00017 | 0.486 |
LIG_SH2_STAT3 | 162 | 165 | PF00017 | 0.258 |
LIG_SH2_STAT5 | 105 | 108 | PF00017 | 0.355 |
LIG_SH2_STAT5 | 162 | 165 | PF00017 | 0.243 |
LIG_SH2_STAT5 | 216 | 219 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 267 | 270 | PF00017 | 0.516 |
LIG_SH2_STAT5 | 482 | 485 | PF00017 | 0.578 |
LIG_SH2_STAT5 | 72 | 75 | PF00017 | 0.589 |
LIG_SH3_1 | 78 | 84 | PF00018 | 0.355 |
LIG_SH3_3 | 449 | 455 | PF00018 | 0.355 |
LIG_SH3_3 | 78 | 84 | PF00018 | 0.355 |
LIG_SUMO_SIM_anti_2 | 539 | 546 | PF11976 | 0.353 |
LIG_SUMO_SIM_par_1 | 17 | 22 | PF11976 | 0.211 |
LIG_SUMO_SIM_par_1 | 317 | 323 | PF11976 | 0.591 |
LIG_WRC_WIRS_1 | 231 | 236 | PF05994 | 0.360 |
LIG_WRC_WIRS_1 | 368 | 373 | PF05994 | 0.416 |
MOD_CK1_1 | 128 | 134 | PF00069 | 0.574 |
MOD_CK1_1 | 358 | 364 | PF00069 | 0.513 |
MOD_CK1_1 | 367 | 373 | PF00069 | 0.482 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.365 |
MOD_CK2_1 | 191 | 197 | PF00069 | 0.489 |
MOD_CK2_1 | 223 | 229 | PF00069 | 0.491 |
MOD_CK2_1 | 286 | 292 | PF00069 | 0.371 |
MOD_CK2_1 | 49 | 55 | PF00069 | 0.519 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.399 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.447 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.403 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.470 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.575 |
MOD_GlcNHglycan | 363 | 366 | PF01048 | 0.487 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.286 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.532 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.353 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.473 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.352 |
MOD_GSK3_1 | 536 | 543 | PF00069 | 0.330 |
MOD_N-GLC_1 | 23 | 28 | PF02516 | 0.317 |
MOD_N-GLC_1 | 274 | 279 | PF02516 | 0.507 |
MOD_N-GLC_1 | 348 | 353 | PF02516 | 0.652 |
MOD_NEK2_1 | 127 | 132 | PF00069 | 0.570 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.337 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.439 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.453 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.490 |
MOD_NEK2_1 | 348 | 353 | PF00069 | 0.679 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.300 |
MOD_NEK2_1 | 380 | 385 | PF00069 | 0.383 |
MOD_NEK2_1 | 420 | 425 | PF00069 | 0.477 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.445 |
MOD_PIKK_1 | 150 | 156 | PF00454 | 0.382 |
MOD_PIKK_1 | 295 | 301 | PF00454 | 0.471 |
MOD_PIKK_1 | 408 | 414 | PF00454 | 0.473 |
MOD_PIKK_1 | 453 | 459 | PF00454 | 0.534 |
MOD_PK_1 | 440 | 446 | PF00069 | 0.454 |
MOD_PKA_2 | 114 | 120 | PF00069 | 0.427 |
MOD_PKA_2 | 210 | 216 | PF00069 | 0.438 |
MOD_PKA_2 | 245 | 251 | PF00069 | 0.433 |
MOD_PKA_2 | 252 | 258 | PF00069 | 0.386 |
MOD_PKA_2 | 295 | 301 | PF00069 | 0.592 |
MOD_PKA_2 | 380 | 386 | PF00069 | 0.377 |
MOD_PKA_2 | 453 | 459 | PF00069 | 0.577 |
MOD_PKA_2 | 480 | 486 | PF00069 | 0.426 |
MOD_Plk_1 | 107 | 113 | PF00069 | 0.399 |
MOD_Plk_1 | 223 | 229 | PF00069 | 0.306 |
MOD_Plk_1 | 23 | 29 | PF00069 | 0.272 |
MOD_Plk_1 | 256 | 262 | PF00069 | 0.459 |
MOD_Plk_1 | 274 | 280 | PF00069 | 0.481 |
MOD_Plk_1 | 322 | 328 | PF00069 | 0.546 |
MOD_Plk_1 | 390 | 396 | PF00069 | 0.405 |
MOD_Plk_2-3 | 191 | 197 | PF00069 | 0.525 |
MOD_Plk_2-3 | 334 | 340 | PF00069 | 0.585 |
MOD_Plk_4 | 191 | 197 | PF00069 | 0.465 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.469 |
MOD_Plk_4 | 274 | 280 | PF00069 | 0.511 |
MOD_Plk_4 | 364 | 370 | PF00069 | 0.606 |
MOD_Plk_4 | 390 | 396 | PF00069 | 0.475 |
MOD_Plk_4 | 444 | 450 | PF00069 | 0.413 |
MOD_Plk_4 | 540 | 546 | PF00069 | 0.358 |
TRG_ENDOCYTIC_2 | 220 | 223 | PF00928 | 0.388 |
TRG_ENDOCYTIC_2 | 72 | 75 | PF00928 | 0.663 |
TRG_ER_diArg_1 | 135 | 137 | PF00400 | 0.272 |
TRG_ER_diArg_1 | 245 | 247 | PF00400 | 0.536 |
TRG_ER_diArg_1 | 32 | 35 | PF00400 | 0.308 |
TRG_ER_diArg_1 | 399 | 402 | PF00400 | 0.406 |
TRG_Pf-PMV_PEXEL_1 | 422 | 427 | PF00026 | 0.372 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I9X5 | Leptomonas seymouri | 66% | 99% |
A0A0S4IQV6 | Bodo saltans | 43% | 98% |
A0A1X0P2R0 | Trypanosomatidae | 49% | 95% |
A0A3Q8IC39 | Leishmania donovani | 82% | 100% |
A0A3R7M632 | Trypanosoma rangeli | 50% | 97% |
A4I5R4 | Leishmania infantum | 82% | 100% |
C9ZR32 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 97% |
E9B109 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
Q4Q757 | Leishmania major | 80% | 100% |
Q9D2H5 | Mus musculus | 23% | 76% |
V5DCZ6 | Trypanosoma cruzi | 51% | 97% |