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: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 2 |
GO:0042995 | cell projection | 2 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 2 |
Related structures:
AlphaFold database: Q4Q757
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 13 |
GO:0008270 | zinc ion binding | 6 | 13 |
GO:0043167 | ion binding | 2 | 13 |
GO:0043169 | cation binding | 3 | 13 |
GO:0046872 | metal ion binding | 4 | 13 |
GO:0046914 | transition metal ion binding | 5 | 13 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 254 | 258 | PF00656 | 0.484 |
CLV_C14_Caspase3-7 | 473 | 477 | PF00656 | 0.662 |
CLV_NRD_NRD_1 | 246 | 248 | PF00675 | 0.492 |
CLV_NRD_NRD_1 | 264 | 266 | PF00675 | 0.477 |
CLV_NRD_NRD_1 | 33 | 35 | PF00675 | 0.348 |
CLV_NRD_NRD_1 | 487 | 489 | PF00675 | 0.600 |
CLV_PCSK_KEX2_1 | 119 | 121 | PF00082 | 0.465 |
CLV_PCSK_KEX2_1 | 246 | 248 | PF00082 | 0.568 |
CLV_PCSK_KEX2_1 | 264 | 266 | PF00082 | 0.553 |
CLV_PCSK_KEX2_1 | 295 | 297 | PF00082 | 0.617 |
CLV_PCSK_KEX2_1 | 33 | 35 | PF00082 | 0.348 |
CLV_PCSK_KEX2_1 | 487 | 489 | PF00082 | 0.600 |
CLV_PCSK_PC1ET2_1 | 119 | 121 | PF00082 | 0.465 |
CLV_PCSK_PC1ET2_1 | 295 | 297 | PF00082 | 0.615 |
CLV_PCSK_PC7_1 | 115 | 121 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 247 | 251 | PF00082 | 0.525 |
CLV_PCSK_SKI1_1 | 34 | 38 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 4 | 8 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 418 | 422 | PF00082 | 0.629 |
DEG_APCC_DBOX_1 | 245 | 253 | PF00400 | 0.507 |
DEG_APCC_DBOX_1 | 264 | 272 | PF00400 | 0.566 |
DOC_CKS1_1 | 376 | 381 | PF01111 | 0.626 |
DOC_CYCLIN_yClb1_LxF_4 | 379 | 384 | PF00134 | 0.501 |
DOC_CYCLIN_yCln2_LP_2 | 15 | 21 | PF00134 | 0.307 |
DOC_CYCLIN_yCln2_LP_2 | 376 | 382 | PF00134 | 0.606 |
DOC_MAPK_MEF2A_6 | 170 | 179 | PF00069 | 0.436 |
DOC_PP1_RVXF_1 | 379 | 385 | PF00149 | 0.507 |
DOC_PP1_RVXF_1 | 495 | 501 | PF00149 | 0.446 |
DOC_PP4_FxxP_1 | 44 | 47 | PF00568 | 0.284 |
DOC_USP7_MATH_1 | 538 | 542 | PF00917 | 0.444 |
DOC_WW_Pin1_4 | 342 | 347 | PF00397 | 0.526 |
DOC_WW_Pin1_4 | 375 | 380 | PF00397 | 0.565 |
DOC_WW_Pin1_4 | 480 | 485 | PF00397 | 0.495 |
LIG_14-3-3_CanoR_1 | 211 | 215 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 246 | 250 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 296 | 304 | PF00244 | 0.569 |
LIG_14-3-3_CanoR_1 | 353 | 360 | PF00244 | 0.738 |
LIG_14-3-3_CanoR_1 | 381 | 385 | PF00244 | 0.472 |
LIG_14-3-3_CanoR_1 | 4 | 12 | PF00244 | 0.356 |
LIG_14-3-3_CanoR_1 | 432 | 438 | PF00244 | 0.509 |
LIG_Actin_WH2_2 | 387 | 404 | PF00022 | 0.448 |
LIG_Actin_WH2_2 | 494 | 512 | PF00022 | 0.461 |
LIG_APCC_ABBA_1 | 102 | 107 | PF00400 | 0.427 |
LIG_APCC_ABBA_1 | 166 | 171 | PF00400 | 0.436 |
LIG_BRCT_BRCA1_1 | 130 | 134 | PF00533 | 0.620 |
LIG_BRCT_BRCA1_1 | 40 | 44 | PF00533 | 0.413 |
LIG_BRCT_BRCA1_1 | 444 | 448 | PF00533 | 0.537 |
LIG_FHA_1 | 174 | 180 | PF00498 | 0.539 |
LIG_FHA_1 | 27 | 33 | PF00498 | 0.377 |
LIG_FHA_1 | 381 | 387 | PF00498 | 0.517 |
LIG_FHA_1 | 481 | 487 | PF00498 | 0.485 |
LIG_FHA_1 | 5 | 11 | PF00498 | 0.323 |
LIG_FHA_2 | 287 | 293 | PF00498 | 0.562 |
LIG_FHA_2 | 325 | 331 | PF00498 | 0.591 |
LIG_KLC1_Yacidic_2 | 70 | 74 | PF13176 | 0.544 |
LIG_LIR_Apic_2 | 41 | 47 | PF02991 | 0.287 |
LIG_LIR_Gen_1 | 217 | 227 | PF02991 | 0.454 |
LIG_LIR_Gen_1 | 228 | 239 | PF02991 | 0.440 |
LIG_LIR_Gen_1 | 419 | 429 | PF02991 | 0.524 |
LIG_LIR_Gen_1 | 69 | 77 | PF02991 | 0.619 |
LIG_LIR_Nem_3 | 217 | 223 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 228 | 234 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 419 | 424 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 445 | 451 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 69 | 75 | PF02991 | 0.573 |
LIG_PDZ_Class_2 | 541 | 546 | PF00595 | 0.425 |
LIG_Rb_pABgroove_1 | 496 | 504 | PF01858 | 0.419 |
LIG_SH2_CRK | 502 | 506 | PF00017 | 0.566 |
LIG_SH2_NCK_1 | 220 | 224 | PF00017 | 0.458 |
LIG_SH2_PTP2 | 72 | 75 | PF00017 | 0.490 |
LIG_SH2_SRC | 64 | 67 | PF00017 | 0.483 |
LIG_SH2_SRC | 72 | 75 | PF00017 | 0.536 |
LIG_SH2_STAP1 | 216 | 220 | PF00017 | 0.591 |
LIG_SH2_STAT3 | 162 | 165 | PF00017 | 0.357 |
LIG_SH2_STAT5 | 105 | 108 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 162 | 165 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 267 | 270 | PF00017 | 0.567 |
LIG_SH2_STAT5 | 482 | 485 | PF00017 | 0.554 |
LIG_SH2_STAT5 | 72 | 75 | PF00017 | 0.544 |
LIG_SH3_2 | 136 | 141 | PF14604 | 0.252 |
LIG_SH3_3 | 133 | 139 | PF00018 | 0.403 |
LIG_SUMO_SIM_anti_2 | 540 | 546 | PF11976 | 0.397 |
LIG_SUMO_SIM_par_1 | 317 | 323 | PF11976 | 0.641 |
MOD_CDK_SPK_2 | 342 | 347 | PF00069 | 0.526 |
MOD_CDK_SPxK_1 | 375 | 381 | PF00069 | 0.587 |
MOD_CDK_SPxxK_3 | 480 | 487 | PF00069 | 0.456 |
MOD_CK1_1 | 128 | 134 | PF00069 | 0.647 |
MOD_CK1_1 | 26 | 32 | PF00069 | 0.385 |
MOD_CK1_1 | 355 | 361 | PF00069 | 0.761 |
MOD_CK1_1 | 456 | 462 | PF00069 | 0.591 |
MOD_CK2_1 | 191 | 197 | PF00069 | 0.544 |
MOD_CK2_1 | 270 | 276 | PF00069 | 0.519 |
MOD_CK2_1 | 286 | 292 | PF00069 | 0.451 |
MOD_CK2_1 | 317 | 323 | PF00069 | 0.710 |
MOD_CK2_1 | 49 | 55 | PF00069 | 0.521 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.480 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.478 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.678 |
MOD_GlcNHglycan | 354 | 357 | PF01048 | 0.658 |
MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.553 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.562 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.603 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.538 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.411 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.654 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.517 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.617 |
MOD_N-GLC_1 | 274 | 279 | PF02516 | 0.526 |
MOD_N-GLC_1 | 340 | 345 | PF02516 | 0.714 |
MOD_N-GLC_1 | 348 | 353 | PF02516 | 0.739 |
MOD_N-GLC_1 | 358 | 363 | PF02516 | 0.722 |
MOD_N-GLC_1 | 38 | 43 | PF02516 | 0.458 |
MOD_N-GLC_1 | 513 | 518 | PF02516 | 0.499 |
MOD_NEK2_1 | 127 | 132 | PF00069 | 0.639 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.395 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.570 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.518 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.589 |
MOD_NEK2_1 | 348 | 353 | PF00069 | 0.762 |
MOD_NEK2_1 | 380 | 385 | PF00069 | 0.490 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.479 |
MOD_NEK2_2 | 366 | 371 | PF00069 | 0.497 |
MOD_PIKK_1 | 150 | 156 | PF00454 | 0.391 |
MOD_PIKK_1 | 295 | 301 | PF00454 | 0.647 |
MOD_PIKK_1 | 408 | 414 | PF00454 | 0.538 |
MOD_PIKK_1 | 453 | 459 | PF00454 | 0.658 |
MOD_PK_1 | 270 | 276 | PF00069 | 0.505 |
MOD_PK_1 | 440 | 446 | PF00069 | 0.506 |
MOD_PKA_1 | 295 | 301 | PF00069 | 0.513 |
MOD_PKA_2 | 114 | 120 | PF00069 | 0.573 |
MOD_PKA_2 | 210 | 216 | PF00069 | 0.533 |
MOD_PKA_2 | 245 | 251 | PF00069 | 0.502 |
MOD_PKA_2 | 252 | 258 | PF00069 | 0.453 |
MOD_PKA_2 | 295 | 301 | PF00069 | 0.619 |
MOD_PKA_2 | 352 | 358 | PF00069 | 0.791 |
MOD_PKA_2 | 380 | 386 | PF00069 | 0.477 |
MOD_PKA_2 | 77 | 83 | PF00069 | 0.606 |
MOD_Plk_1 | 274 | 280 | PF00069 | 0.500 |
MOD_Plk_1 | 322 | 328 | PF00069 | 0.615 |
MOD_Plk_1 | 358 | 364 | PF00069 | 0.638 |
MOD_Plk_1 | 390 | 396 | PF00069 | 0.462 |
MOD_Plk_2-3 | 191 | 197 | PF00069 | 0.573 |
MOD_Plk_2-3 | 334 | 340 | PF00069 | 0.675 |
MOD_Plk_4 | 191 | 197 | PF00069 | 0.513 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.391 |
MOD_Plk_4 | 274 | 280 | PF00069 | 0.563 |
MOD_Plk_4 | 366 | 372 | PF00069 | 0.685 |
MOD_Plk_4 | 390 | 396 | PF00069 | 0.536 |
MOD_Plk_4 | 444 | 450 | PF00069 | 0.450 |
MOD_Plk_4 | 540 | 546 | PF00069 | 0.364 |
MOD_ProDKin_1 | 342 | 348 | PF00069 | 0.527 |
MOD_ProDKin_1 | 375 | 381 | PF00069 | 0.561 |
MOD_ProDKin_1 | 480 | 486 | PF00069 | 0.494 |
TRG_ENDOCYTIC_2 | 220 | 223 | PF00928 | 0.459 |
TRG_ENDOCYTIC_2 | 502 | 505 | PF00928 | 0.559 |
TRG_ENDOCYTIC_2 | 72 | 75 | PF00928 | 0.620 |
TRG_ER_diArg_1 | 245 | 247 | PF00400 | 0.601 |
TRG_ER_diArg_1 | 32 | 34 | PF00400 | 0.411 |
TRG_ER_diArg_1 | 399 | 402 | PF00400 | 0.587 |
TRG_ER_diArg_1 | 486 | 488 | PF00400 | 0.593 |
TRG_ER_diArg_1 | 497 | 500 | PF00400 | 0.496 |
TRG_Pf-PMV_PEXEL_1 | 34 | 38 | PF00026 | 0.346 |
TRG_Pf-PMV_PEXEL_1 | 499 | 503 | PF00026 | 0.411 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I9X5 | Leptomonas seymouri | 68% | 99% |
A0A0S4IQV6 | Bodo saltans | 44% | 98% |
A0A0S4JR35 | Bodo saltans | 24% | 91% |
A0A1X0P2R0 | Trypanosomatidae | 51% | 95% |
A0A3Q8IC39 | Leishmania donovani | 95% | 100% |
A0A3R7M632 | Trypanosoma rangeli | 52% | 97% |
A4HIG8 | Leishmania braziliensis | 80% | 100% |
A4I5R4 | Leishmania infantum | 95% | 100% |
C9ZR32 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 97% |
E9B109 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
V5DCZ6 | Trypanosoma cruzi | 53% | 97% |