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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A4HL40
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 128 | 132 | PF00656 | 0.500 |
CLV_C14_Caspase3-7 | 447 | 451 | PF00656 | 0.537 |
CLV_C14_Caspase3-7 | 516 | 520 | PF00656 | 0.676 |
CLV_C14_Caspase3-7 | 68 | 72 | PF00656 | 0.509 |
CLV_NRD_NRD_1 | 153 | 155 | PF00675 | 0.531 |
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.608 |
CLV_NRD_NRD_1 | 339 | 341 | PF00675 | 0.673 |
CLV_NRD_NRD_1 | 412 | 414 | PF00675 | 0.736 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.572 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.608 |
CLV_PCSK_KEX2_1 | 338 | 340 | PF00082 | 0.682 |
CLV_PCSK_KEX2_1 | 412 | 414 | PF00082 | 0.702 |
CLV_PCSK_KEX2_1 | 454 | 456 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 88 | 90 | PF00082 | 0.572 |
CLV_PCSK_PC1ET2_1 | 454 | 456 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 18 | 22 | PF00082 | 0.483 |
CLV_PCSK_SKI1_1 | 217 | 221 | PF00082 | 0.544 |
CLV_PCSK_SKI1_1 | 307 | 311 | PF00082 | 0.654 |
CLV_PCSK_SKI1_1 | 89 | 93 | PF00082 | 0.587 |
DEG_APCC_DBOX_1 | 17 | 25 | PF00400 | 0.507 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.723 |
DEG_SPOP_SBC_1 | 506 | 510 | PF00917 | 0.427 |
DOC_CYCLIN_RxL_1 | 112 | 121 | PF00134 | 0.426 |
DOC_CYCLIN_RxL_1 | 214 | 224 | PF00134 | 0.538 |
DOC_MAPK_gen_1 | 214 | 222 | PF00069 | 0.410 |
DOC_MAPK_MEF2A_6 | 214 | 222 | PF00069 | 0.447 |
DOC_PP1_RVXF_1 | 114 | 121 | PF00149 | 0.418 |
DOC_USP7_MATH_1 | 159 | 163 | PF00917 | 0.549 |
DOC_USP7_MATH_1 | 260 | 264 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 266 | 270 | PF00917 | 0.726 |
DOC_USP7_MATH_1 | 478 | 482 | PF00917 | 0.471 |
DOC_USP7_MATH_1 | 486 | 490 | PF00917 | 0.452 |
DOC_USP7_MATH_1 | 506 | 510 | PF00917 | 0.427 |
DOC_WW_Pin1_4 | 137 | 142 | PF00397 | 0.702 |
DOC_WW_Pin1_4 | 360 | 365 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 368 | 373 | PF00397 | 0.532 |
DOC_WW_Pin1_4 | 390 | 395 | PF00397 | 0.656 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.429 |
LIG_14-3-3_CanoR_1 | 11 | 20 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 2 | 6 | PF00244 | 0.666 |
LIG_14-3-3_CanoR_1 | 76 | 85 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 88 | 94 | PF00244 | 0.573 |
LIG_BRCT_BRCA1_1 | 391 | 395 | PF00533 | 0.537 |
LIG_BRCT_BRCA1_1 | 51 | 55 | PF00533 | 0.482 |
LIG_EVH1_2 | 141 | 145 | PF00568 | 0.471 |
LIG_FHA_1 | 108 | 114 | PF00498 | 0.292 |
LIG_FHA_1 | 138 | 144 | PF00498 | 0.566 |
LIG_FHA_1 | 148 | 154 | PF00498 | 0.667 |
LIG_FHA_1 | 194 | 200 | PF00498 | 0.453 |
LIG_FHA_1 | 30 | 36 | PF00498 | 0.334 |
LIG_FHA_1 | 339 | 345 | PF00498 | 0.701 |
LIG_FHA_1 | 444 | 450 | PF00498 | 0.680 |
LIG_FHA_2 | 124 | 130 | PF00498 | 0.659 |
LIG_FHA_2 | 300 | 306 | PF00498 | 0.538 |
LIG_FHA_2 | 438 | 444 | PF00498 | 0.634 |
LIG_FHA_2 | 483 | 489 | PF00498 | 0.582 |
LIG_FHA_2 | 514 | 520 | PF00498 | 0.631 |
LIG_FHA_2 | 55 | 61 | PF00498 | 0.569 |
LIG_FHA_2 | 66 | 72 | PF00498 | 0.371 |
LIG_HCF-1_HBM_1 | 200 | 203 | PF13415 | 0.532 |
LIG_LIR_Apic_2 | 366 | 372 | PF02991 | 0.494 |
LIG_LIR_Gen_1 | 117 | 125 | PF02991 | 0.455 |
LIG_LIR_Gen_1 | 393 | 400 | PF02991 | 0.533 |
LIG_LIR_Nem_3 | 14 | 20 | PF02991 | 0.551 |
LIG_LIR_Nem_3 | 224 | 229 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 393 | 399 | PF02991 | 0.550 |
LIG_Pex14_2 | 51 | 55 | PF04695 | 0.400 |
LIG_SH2_CRK | 31 | 35 | PF00017 | 0.537 |
LIG_SH2_SRC | 448 | 451 | PF00017 | 0.536 |
LIG_SH2_STAP1 | 31 | 35 | PF00017 | 0.329 |
LIG_SH2_STAT3 | 144 | 147 | PF00017 | 0.433 |
LIG_SH2_STAT3 | 203 | 206 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 144 | 147 | PF00017 | 0.433 |
LIG_SH2_STAT5 | 245 | 248 | PF00017 | 0.556 |
LIG_SH2_STAT5 | 31 | 34 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 448 | 451 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 483 | 486 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 77 | 80 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.489 |
LIG_SH3_2 | 209 | 214 | PF14604 | 0.465 |
LIG_SH3_3 | 206 | 212 | PF00018 | 0.494 |
LIG_SH3_3 | 256 | 262 | PF00018 | 0.692 |
LIG_SH3_3 | 33 | 39 | PF00018 | 0.579 |
LIG_SH3_3 | 358 | 364 | PF00018 | 0.508 |
LIG_SH3_3 | 417 | 423 | PF00018 | 0.612 |
LIG_SH3_3 | 47 | 53 | PF00018 | 0.551 |
LIG_SUMO_SIM_anti_2 | 291 | 297 | PF11976 | 0.613 |
LIG_TRAF2_1 | 371 | 374 | PF00917 | 0.663 |
LIG_TYR_ITIM | 29 | 34 | PF00017 | 0.532 |
LIG_WW_1 | 141 | 144 | PF00397 | 0.429 |
MOD_CDK_SPxxK_3 | 368 | 375 | PF00069 | 0.448 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.684 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.317 |
MOD_CK1_1 | 318 | 324 | PF00069 | 0.707 |
MOD_CK1_1 | 363 | 369 | PF00069 | 0.616 |
MOD_CK1_1 | 481 | 487 | PF00069 | 0.420 |
MOD_CK2_1 | 123 | 129 | PF00069 | 0.631 |
MOD_CK2_1 | 251 | 257 | PF00069 | 0.648 |
MOD_CK2_1 | 299 | 305 | PF00069 | 0.600 |
MOD_CK2_1 | 368 | 374 | PF00069 | 0.659 |
MOD_CK2_1 | 400 | 406 | PF00069 | 0.661 |
MOD_CK2_1 | 437 | 443 | PF00069 | 0.579 |
MOD_CK2_1 | 482 | 488 | PF00069 | 0.554 |
MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.431 |
MOD_GlcNHglycan | 136 | 140 | PF01048 | 0.699 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.518 |
MOD_GlcNHglycan | 355 | 358 | PF01048 | 0.687 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.582 |
MOD_GlcNHglycan | 488 | 491 | PF01048 | 0.462 |
MOD_GlcNHglycan | 509 | 512 | PF01048 | 0.579 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.506 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.684 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.502 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.667 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.485 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.724 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.568 |
MOD_GSK3_1 | 477 | 484 | PF00069 | 0.519 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.371 |
MOD_GSK3_1 | 501 | 508 | PF00069 | 0.425 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.489 |
MOD_LATS_1 | 9 | 15 | PF00433 | 0.361 |
MOD_N-GLC_1 | 29 | 34 | PF02516 | 0.342 |
MOD_N-GLC_1 | 89 | 94 | PF02516 | 0.424 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.728 |
MOD_NEK2_1 | 299 | 304 | PF00069 | 0.507 |
MOD_NEK2_1 | 319 | 324 | PF00069 | 0.612 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.578 |
MOD_NEK2_1 | 460 | 465 | PF00069 | 0.481 |
MOD_NEK2_1 | 505 | 510 | PF00069 | 0.460 |
MOD_NEK2_1 | 54 | 59 | PF00069 | 0.469 |
MOD_PIKK_1 | 177 | 183 | PF00454 | 0.338 |
MOD_PIKK_1 | 400 | 406 | PF00454 | 0.622 |
MOD_PIKK_1 | 54 | 60 | PF00454 | 0.588 |
MOD_PKA_1 | 338 | 344 | PF00069 | 0.707 |
MOD_PKA_2 | 1 | 7 | PF00069 | 0.697 |
MOD_PKA_2 | 213 | 219 | PF00069 | 0.413 |
MOD_PKA_2 | 338 | 344 | PF00069 | 0.674 |
MOD_PKA_2 | 411 | 417 | PF00069 | 0.702 |
MOD_PKA_2 | 481 | 487 | PF00069 | 0.476 |
MOD_Plk_1 | 29 | 35 | PF00069 | 0.338 |
MOD_Plk_1 | 291 | 297 | PF00069 | 0.546 |
MOD_Plk_1 | 373 | 379 | PF00069 | 0.557 |
MOD_Plk_1 | 460 | 466 | PF00069 | 0.483 |
MOD_Plk_1 | 89 | 95 | PF00069 | 0.335 |
MOD_Plk_4 | 291 | 297 | PF00069 | 0.539 |
MOD_Plk_4 | 30 | 36 | PF00069 | 0.593 |
MOD_Plk_4 | 315 | 321 | PF00069 | 0.649 |
MOD_ProDKin_1 | 137 | 143 | PF00069 | 0.698 |
MOD_ProDKin_1 | 360 | 366 | PF00069 | 0.662 |
MOD_ProDKin_1 | 368 | 374 | PF00069 | 0.530 |
MOD_ProDKin_1 | 390 | 396 | PF00069 | 0.648 |
MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.428 |
MOD_SUMO_rev_2 | 300 | 309 | PF00179 | 0.469 |
TRG_ENDOCYTIC_2 | 17 | 20 | PF00928 | 0.508 |
TRG_ENDOCYTIC_2 | 31 | 34 | PF00928 | 0.543 |
TRG_ENDOCYTIC_2 | 426 | 429 | PF00928 | 0.667 |
TRG_ER_diArg_1 | 1 | 3 | PF00400 | 0.616 |
TRG_ER_diArg_1 | 248 | 251 | PF00400 | 0.666 |
TRG_ER_diArg_1 | 337 | 340 | PF00400 | 0.645 |
TRG_ER_diArg_1 | 411 | 413 | PF00400 | 0.736 |
TRG_Pf-PMV_PEXEL_1 | 250 | 255 | PF00026 | 0.487 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKK4 | Leptomonas seymouri | 60% | 99% |
A0A0S4JPU3 | Bodo saltans | 33% | 95% |
A0A3S7X6B5 | Leishmania donovani | 79% | 100% |
A0A422NYF9 | Trypanosoma rangeli | 43% | 100% |
A4I8M0 | Leishmania infantum | 79% | 100% |
C9ZPU4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 98% |
E9B3I1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 100% |
Q4Q4L9 | Leishmania major | 77% | 100% |
V5AUZ3 | Trypanosoma cruzi | 45% | 100% |