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: A4HBP8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 317 | 321 | PF00656 | 0.503 |
CLV_C14_Caspase3-7 | 50 | 54 | PF00656 | 0.472 |
CLV_NRD_NRD_1 | 256 | 258 | PF00675 | 0.482 |
CLV_NRD_NRD_1 | 449 | 451 | PF00675 | 0.637 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.403 |
CLV_PCSK_KEX2_1 | 448 | 450 | PF00082 | 0.642 |
CLV_PCSK_KEX2_1 | 84 | 86 | PF00082 | 0.742 |
CLV_PCSK_PC1ET2_1 | 142 | 144 | PF00082 | 0.515 |
CLV_PCSK_PC1ET2_1 | 448 | 450 | PF00082 | 0.763 |
CLV_PCSK_PC1ET2_1 | 84 | 86 | PF00082 | 0.742 |
CLV_PCSK_SKI1_1 | 143 | 147 | PF00082 | 0.423 |
CLV_PCSK_SKI1_1 | 29 | 33 | PF00082 | 0.644 |
CLV_PCSK_SKI1_1 | 37 | 41 | PF00082 | 0.525 |
CLV_PCSK_SKI1_1 | 398 | 402 | PF00082 | 0.728 |
CLV_PCSK_SKI1_1 | 494 | 498 | PF00082 | 0.524 |
DEG_APCC_DBOX_1 | 142 | 150 | PF00400 | 0.412 |
DEG_SCF_FBW7_1 | 148 | 154 | PF00400 | 0.530 |
DEG_SPOP_SBC_1 | 76 | 80 | PF00917 | 0.643 |
DOC_CDC14_PxL_1 | 131 | 139 | PF14671 | 0.536 |
DOC_CDC14_PxL_1 | 192 | 200 | PF14671 | 0.558 |
DOC_CKS1_1 | 148 | 153 | PF01111 | 0.494 |
DOC_CKS1_1 | 462 | 467 | PF01111 | 0.704 |
DOC_CKS1_1 | 469 | 474 | PF01111 | 0.685 |
DOC_CKS1_1 | 520 | 525 | PF01111 | 0.634 |
DOC_CYCLIN_yCln2_LP_2 | 198 | 201 | PF00134 | 0.598 |
DOC_CYCLIN_yCln2_LP_2 | 428 | 434 | PF00134 | 0.599 |
DOC_MAPK_gen_1 | 142 | 148 | PF00069 | 0.402 |
DOC_PP2B_LxvP_1 | 193 | 196 | PF13499 | 0.509 |
DOC_PP2B_LxvP_1 | 198 | 201 | PF13499 | 0.520 |
DOC_PP4_MxPP_1 | 470 | 473 | PF00568 | 0.619 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.696 |
DOC_USP7_MATH_1 | 240 | 244 | PF00917 | 0.452 |
DOC_USP7_MATH_1 | 480 | 484 | PF00917 | 0.616 |
DOC_USP7_MATH_1 | 505 | 509 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 528 | 532 | PF00917 | 0.687 |
DOC_WW_Pin1_4 | 147 | 152 | PF00397 | 0.434 |
DOC_WW_Pin1_4 | 461 | 466 | PF00397 | 0.641 |
DOC_WW_Pin1_4 | 468 | 473 | PF00397 | 0.675 |
DOC_WW_Pin1_4 | 508 | 513 | PF00397 | 0.699 |
DOC_WW_Pin1_4 | 519 | 524 | PF00397 | 0.663 |
DOC_WW_Pin1_4 | 77 | 82 | PF00397 | 0.717 |
LIG_14-3-3_CanoR_1 | 37 | 46 | PF00244 | 0.587 |
LIG_14-3-3_CanoR_1 | 449 | 453 | PF00244 | 0.664 |
LIG_14-3-3_CanoR_1 | 8 | 13 | PF00244 | 0.746 |
LIG_Actin_WH2_2 | 127 | 144 | PF00022 | 0.560 |
LIG_Actin_WH2_2 | 68 | 86 | PF00022 | 0.470 |
LIG_APCC_ABBA_1 | 227 | 232 | PF00400 | 0.440 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.702 |
LIG_BIR_III_4 | 320 | 324 | PF00653 | 0.499 |
LIG_BRCT_BRCA1_1 | 304 | 308 | PF00533 | 0.635 |
LIG_CaM_IQ_9 | 241 | 256 | PF13499 | 0.402 |
LIG_FHA_1 | 148 | 154 | PF00498 | 0.493 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.511 |
LIG_FHA_1 | 219 | 225 | PF00498 | 0.649 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.516 |
LIG_FHA_1 | 361 | 367 | PF00498 | 0.569 |
LIG_FHA_1 | 409 | 415 | PF00498 | 0.570 |
LIG_FHA_2 | 315 | 321 | PF00498 | 0.504 |
LIG_FHA_2 | 38 | 44 | PF00498 | 0.519 |
LIG_FHA_2 | 542 | 548 | PF00498 | 0.614 |
LIG_LIR_Gen_1 | 109 | 119 | PF02991 | 0.442 |
LIG_LIR_Gen_1 | 157 | 165 | PF02991 | 0.498 |
LIG_LIR_Gen_1 | 205 | 215 | PF02991 | 0.561 |
LIG_LIR_Gen_1 | 344 | 354 | PF02991 | 0.332 |
LIG_LIR_Gen_1 | 43 | 52 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 157 | 162 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 205 | 210 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 344 | 349 | PF02991 | 0.301 |
LIG_LIR_Nem_3 | 43 | 49 | PF02991 | 0.330 |
LIG_MYND_1 | 196 | 200 | PF01753 | 0.619 |
LIG_MYND_1 | 435 | 439 | PF01753 | 0.632 |
LIG_MYND_3 | 134 | 138 | PF01753 | 0.531 |
LIG_NRBOX | 176 | 182 | PF00104 | 0.429 |
LIG_NRBOX | 223 | 229 | PF00104 | 0.644 |
LIG_SH2_CRK | 119 | 123 | PF00017 | 0.508 |
LIG_SH2_NCK_1 | 203 | 207 | PF00017 | 0.402 |
LIG_SH2_PTP2 | 516 | 519 | PF00017 | 0.541 |
LIG_SH2_SRC | 203 | 206 | PF00017 | 0.623 |
LIG_SH2_SRC | 272 | 275 | PF00017 | 0.431 |
LIG_SH2_SRC | 516 | 519 | PF00017 | 0.541 |
LIG_SH2_STAP1 | 203 | 207 | PF00017 | 0.616 |
LIG_SH2_STAT3 | 129 | 132 | PF00017 | 0.422 |
LIG_SH2_STAT3 | 62 | 65 | PF00017 | 0.568 |
LIG_SH2_STAT5 | 272 | 275 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 298 | 301 | PF00017 | 0.609 |
LIG_SH2_STAT5 | 516 | 519 | PF00017 | 0.739 |
LIG_SH3_3 | 145 | 151 | PF00018 | 0.419 |
LIG_SH3_3 | 349 | 355 | PF00018 | 0.532 |
LIG_SH3_3 | 403 | 409 | PF00018 | 0.691 |
LIG_SH3_3 | 429 | 435 | PF00018 | 0.629 |
LIG_SH3_3 | 451 | 457 | PF00018 | 0.700 |
LIG_SH3_3 | 459 | 465 | PF00018 | 0.657 |
LIG_SH3_3 | 466 | 472 | PF00018 | 0.605 |
LIG_SH3_3 | 482 | 488 | PF00018 | 0.760 |
LIG_SH3_3 | 517 | 523 | PF00018 | 0.687 |
LIG_Sin3_3 | 440 | 447 | PF02671 | 0.745 |
LIG_SUMO_SIM_par_1 | 189 | 194 | PF11976 | 0.561 |
LIG_TRAF2_1 | 300 | 303 | PF00917 | 0.636 |
LIG_TRAF2_1 | 382 | 385 | PF00917 | 0.507 |
LIG_TRAF2_1 | 40 | 43 | PF00917 | 0.577 |
LIG_TYR_ITIM | 117 | 122 | PF00017 | 0.516 |
LIG_UBA3_1 | 133 | 142 | PF00899 | 0.518 |
LIG_WW_1 | 200 | 203 | PF00397 | 0.368 |
MOD_CDK_SPxxK_3 | 508 | 515 | PF00069 | 0.533 |
MOD_CDK_SPxxK_3 | 77 | 84 | PF00069 | 0.712 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.703 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.451 |
MOD_CK1_1 | 508 | 514 | PF00069 | 0.633 |
MOD_CK2_1 | 151 | 157 | PF00069 | 0.449 |
MOD_CK2_1 | 20 | 26 | PF00069 | 0.675 |
MOD_CK2_1 | 297 | 303 | PF00069 | 0.566 |
MOD_CK2_1 | 37 | 43 | PF00069 | 0.526 |
MOD_CK2_1 | 378 | 384 | PF00069 | 0.610 |
MOD_Cter_Amidation | 396 | 399 | PF01082 | 0.564 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.526 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.746 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.665 |
MOD_GlcNHglycan | 303 | 307 | PF01048 | 0.471 |
MOD_GlcNHglycan | 380 | 383 | PF01048 | 0.467 |
MOD_GlcNHglycan | 401 | 404 | PF01048 | 0.693 |
MOD_GlcNHglycan | 465 | 468 | PF01048 | 0.713 |
MOD_GlcNHglycan | 498 | 501 | PF01048 | 0.579 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.741 |
MOD_GlcNHglycan | 530 | 533 | PF01048 | 0.725 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.480 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.491 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.649 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.751 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.676 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.566 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.721 |
MOD_LATS_1 | 96 | 102 | PF00433 | 0.510 |
MOD_N-GLC_1 | 217 | 222 | PF02516 | 0.579 |
MOD_NEK2_1 | 164 | 169 | PF00069 | 0.402 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.477 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.643 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.506 |
MOD_NEK2_1 | 97 | 102 | PF00069 | 0.734 |
MOD_PIKK_1 | 390 | 396 | PF00454 | 0.773 |
MOD_PK_1 | 8 | 14 | PF00069 | 0.745 |
MOD_PKA_1 | 3 | 9 | PF00069 | 0.533 |
MOD_PKA_1 | 398 | 404 | PF00069 | 0.726 |
MOD_PKA_1 | 448 | 454 | PF00069 | 0.697 |
MOD_PKA_2 | 448 | 454 | PF00069 | 0.673 |
MOD_PKA_2 | 7 | 13 | PF00069 | 0.538 |
MOD_Plk_1 | 494 | 500 | PF00069 | 0.650 |
MOD_Plk_4 | 180 | 186 | PF00069 | 0.495 |
MOD_ProDKin_1 | 147 | 153 | PF00069 | 0.433 |
MOD_ProDKin_1 | 461 | 467 | PF00069 | 0.642 |
MOD_ProDKin_1 | 468 | 474 | PF00069 | 0.672 |
MOD_ProDKin_1 | 508 | 514 | PF00069 | 0.703 |
MOD_ProDKin_1 | 519 | 525 | PF00069 | 0.662 |
MOD_ProDKin_1 | 77 | 83 | PF00069 | 0.722 |
TRG_DiLeu_BaEn_1 | 187 | 192 | PF01217 | 0.502 |
TRG_DiLeu_BaEn_2 | 343 | 349 | PF01217 | 0.269 |
TRG_DiLeu_BaLyEn_6 | 403 | 408 | PF01217 | 0.741 |
TRG_ENDOCYTIC_2 | 119 | 122 | PF00928 | 0.471 |
TRG_ENDOCYTIC_2 | 46 | 49 | PF00928 | 0.321 |
TRG_NLS_MonoExtN_4 | 254 | 261 | PF00514 | 0.525 |
TRG_NLS_MonoExtN_4 | 446 | 452 | PF00514 | 0.760 |
TRG_Pf-PMV_PEXEL_1 | 260 | 264 | PF00026 | 0.469 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IAT9 | Leptomonas seymouri | 58% | 94% |
A0A1X0NXH4 | Trypanosomatidae | 25% | 100% |
A0A3Q8IAT2 | Leishmania donovani | 83% | 100% |
A0A422NBI2 | Trypanosoma rangeli | 29% | 100% |
A4HZ50 | Leishmania infantum | 75% | 95% |
D0A1Q2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9AV18 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 99% |
Q4QCG4 | Leishmania major | 73% | 96% |
V5BKP0 | Trypanosoma cruzi | 28% | 100% |