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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: A4HP88
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 109 | 113 | PF00656 | 0.567 |
CLV_C14_Caspase3-7 | 98 | 102 | PF00656 | 0.632 |
CLV_NRD_NRD_1 | 133 | 135 | PF00675 | 0.533 |
CLV_NRD_NRD_1 | 213 | 215 | PF00675 | 0.754 |
CLV_NRD_NRD_1 | 312 | 314 | PF00675 | 0.729 |
CLV_NRD_NRD_1 | 359 | 361 | PF00675 | 0.616 |
CLV_NRD_NRD_1 | 485 | 487 | PF00675 | 0.710 |
CLV_NRD_NRD_1 | 506 | 508 | PF00675 | 0.550 |
CLV_NRD_NRD_1 | 520 | 522 | PF00675 | 0.491 |
CLV_NRD_NRD_1 | 566 | 568 | PF00675 | 0.557 |
CLV_NRD_NRD_1 | 570 | 572 | PF00675 | 0.567 |
CLV_PCSK_FUR_1 | 518 | 522 | PF00082 | 0.469 |
CLV_PCSK_KEX2_1 | 205 | 207 | PF00082 | 0.669 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.685 |
CLV_PCSK_KEX2_1 | 442 | 444 | PF00082 | 0.658 |
CLV_PCSK_KEX2_1 | 485 | 487 | PF00082 | 0.710 |
CLV_PCSK_KEX2_1 | 520 | 522 | PF00082 | 0.583 |
CLV_PCSK_PC1ET2_1 | 205 | 207 | PF00082 | 0.631 |
CLV_PCSK_PC1ET2_1 | 442 | 444 | PF00082 | 0.661 |
CLV_PCSK_PC7_1 | 438 | 444 | PF00082 | 0.543 |
CLV_PCSK_PC7_1 | 516 | 522 | PF00082 | 0.461 |
CLV_PCSK_SKI1_1 | 269 | 273 | PF00082 | 0.469 |
CLV_PCSK_SKI1_1 | 431 | 435 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 464 | 468 | PF00082 | 0.637 |
CLV_PCSK_SKI1_1 | 576 | 580 | PF00082 | 0.694 |
CLV_PCSK_SKI1_1 | 87 | 91 | PF00082 | 0.579 |
DEG_APCC_DBOX_1 | 570 | 578 | PF00400 | 0.568 |
DEG_SCF_FBW7_2 | 222 | 227 | PF00400 | 0.496 |
DOC_CYCLIN_RxL_1 | 406 | 418 | PF00134 | 0.477 |
DOC_PP4_FxxP_1 | 585 | 588 | PF00568 | 0.616 |
DOC_USP7_MATH_1 | 147 | 151 | PF00917 | 0.560 |
DOC_USP7_MATH_1 | 307 | 311 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 481 | 485 | PF00917 | 0.572 |
DOC_USP7_UBL2_3 | 265 | 269 | PF12436 | 0.458 |
DOC_USP7_UBL2_3 | 564 | 568 | PF12436 | 0.606 |
DOC_USP7_UBL2_3 | 572 | 576 | PF12436 | 0.514 |
DOC_WW_Pin1_4 | 218 | 223 | PF00397 | 0.668 |
DOC_WW_Pin1_4 | 301 | 306 | PF00397 | 0.627 |
DOC_WW_Pin1_4 | 456 | 461 | PF00397 | 0.666 |
LIG_14-3-3_CanoR_1 | 125 | 129 | PF00244 | 0.543 |
LIG_14-3-3_CanoR_1 | 134 | 140 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 141 | 147 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 366 | 370 | PF00244 | 0.580 |
LIG_14-3-3_CanoR_1 | 507 | 511 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 76 | 81 | PF00244 | 0.592 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.798 |
LIG_EVH1_1 | 585 | 589 | PF00568 | 0.639 |
LIG_EVH1_1 | 69 | 73 | PF00568 | 0.542 |
LIG_FHA_1 | 182 | 188 | PF00498 | 0.497 |
LIG_FHA_1 | 270 | 276 | PF00498 | 0.733 |
LIG_FHA_1 | 30 | 36 | PF00498 | 0.660 |
LIG_FHA_1 | 323 | 329 | PF00498 | 0.518 |
LIG_FHA_1 | 37 | 43 | PF00498 | 0.606 |
LIG_FHA_1 | 421 | 427 | PF00498 | 0.515 |
LIG_FHA_2 | 416 | 422 | PF00498 | 0.535 |
LIG_FHA_2 | 457 | 463 | PF00498 | 0.582 |
LIG_FHA_2 | 77 | 83 | PF00498 | 0.757 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.589 |
LIG_LIR_Gen_1 | 472 | 482 | PF02991 | 0.517 |
LIG_LIR_Gen_1 | 509 | 514 | PF02991 | 0.598 |
LIG_LIR_Nem_3 | 472 | 477 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 509 | 513 | PF02991 | 0.600 |
LIG_NRBOX | 228 | 234 | PF00104 | 0.626 |
LIG_Pex14_1 | 506 | 510 | PF04695 | 0.551 |
LIG_Pex14_2 | 259 | 263 | PF04695 | 0.620 |
LIG_PTAP_UEV_1 | 236 | 241 | PF05743 | 0.512 |
LIG_RPA_C_Fungi | 136 | 148 | PF08784 | 0.495 |
LIG_SH2_CRK | 510 | 514 | PF00017 | 0.605 |
LIG_SH2_STAP1 | 346 | 350 | PF00017 | 0.594 |
LIG_SH2_STAP1 | 49 | 53 | PF00017 | 0.558 |
LIG_SH2_STAP1 | 510 | 514 | PF00017 | 0.549 |
LIG_SH2_STAT3 | 117 | 120 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 117 | 120 | PF00017 | 0.530 |
LIG_SH3_2 | 10 | 15 | PF14604 | 0.668 |
LIG_SH3_2 | 237 | 242 | PF14604 | 0.633 |
LIG_SH3_2 | 586 | 591 | PF14604 | 0.513 |
LIG_SH3_3 | 219 | 225 | PF00018 | 0.658 |
LIG_SH3_3 | 234 | 240 | PF00018 | 0.622 |
LIG_SH3_3 | 285 | 291 | PF00018 | 0.558 |
LIG_SH3_3 | 457 | 463 | PF00018 | 0.523 |
LIG_SH3_3 | 583 | 589 | PF00018 | 0.629 |
LIG_SH3_3 | 64 | 70 | PF00018 | 0.604 |
LIG_SH3_3 | 7 | 13 | PF00018 | 0.793 |
LIG_SUMO_SIM_par_1 | 32 | 39 | PF11976 | 0.550 |
LIG_SUMO_SIM_par_1 | 59 | 65 | PF11976 | 0.575 |
LIG_TRAF2_1 | 459 | 462 | PF00917 | 0.517 |
LIG_TRFH_1 | 585 | 589 | PF08558 | 0.555 |
MOD_CDK_SPxxK_3 | 301 | 308 | PF00069 | 0.625 |
MOD_CK1_1 | 509 | 515 | PF00069 | 0.410 |
MOD_CK1_1 | 51 | 57 | PF00069 | 0.640 |
MOD_CK2_1 | 415 | 421 | PF00069 | 0.554 |
MOD_CK2_1 | 456 | 462 | PF00069 | 0.531 |
MOD_CK2_1 | 481 | 487 | PF00069 | 0.580 |
MOD_CK2_1 | 528 | 534 | PF00069 | 0.624 |
MOD_CK2_1 | 76 | 82 | PF00069 | 0.690 |
MOD_GlcNHglycan | 169 | 173 | PF01048 | 0.636 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.521 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.610 |
MOD_GlcNHglycan | 27 | 32 | PF01048 | 0.691 |
MOD_GlcNHglycan | 479 | 482 | PF01048 | 0.607 |
MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.662 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.481 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.540 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.680 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.652 |
MOD_GSK3_1 | 411 | 418 | PF00069 | 0.530 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.662 |
MOD_GSK3_1 | 477 | 484 | PF00069 | 0.575 |
MOD_GSK3_1 | 502 | 509 | PF00069 | 0.481 |
MOD_N-GLC_1 | 301 | 306 | PF02516 | 0.571 |
MOD_N-GLC_2 | 183 | 185 | PF02516 | 0.526 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.558 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.595 |
MOD_NEK2_1 | 369 | 374 | PF00069 | 0.524 |
MOD_NEK2_1 | 415 | 420 | PF00069 | 0.488 |
MOD_PIKK_1 | 308 | 314 | PF00454 | 0.586 |
MOD_PIKK_1 | 433 | 439 | PF00454 | 0.538 |
MOD_PIKK_1 | 489 | 495 | PF00454 | 0.456 |
MOD_PKA_1 | 360 | 366 | PF00069 | 0.623 |
MOD_PKA_1 | 411 | 417 | PF00069 | 0.620 |
MOD_PKA_2 | 124 | 130 | PF00069 | 0.554 |
MOD_PKA_2 | 307 | 313 | PF00069 | 0.606 |
MOD_PKA_2 | 365 | 371 | PF00069 | 0.605 |
MOD_PKA_2 | 506 | 512 | PF00069 | 0.550 |
MOD_PKA_2 | 75 | 81 | PF00069 | 0.706 |
MOD_PKA_2 | 91 | 97 | PF00069 | 0.570 |
MOD_Plk_2-3 | 97 | 103 | PF00069 | 0.590 |
MOD_Plk_4 | 365 | 371 | PF00069 | 0.525 |
MOD_Plk_4 | 411 | 417 | PF00069 | 0.620 |
MOD_Plk_4 | 509 | 515 | PF00069 | 0.410 |
MOD_ProDKin_1 | 218 | 224 | PF00069 | 0.662 |
MOD_ProDKin_1 | 301 | 307 | PF00069 | 0.621 |
MOD_ProDKin_1 | 456 | 462 | PF00069 | 0.661 |
MOD_SUMO_rev_2 | 457 | 466 | PF00179 | 0.656 |
TRG_DiLeu_BaEn_3 | 158 | 164 | PF01217 | 0.650 |
TRG_ENDOCYTIC_2 | 346 | 349 | PF00928 | 0.594 |
TRG_ENDOCYTIC_2 | 510 | 513 | PF00928 | 0.608 |
TRG_ER_diArg_1 | 200 | 203 | PF00400 | 0.487 |
TRG_ER_diArg_1 | 518 | 521 | PF00400 | 0.467 |
TRG_NLS_MonoExtC_3 | 440 | 446 | PF00514 | 0.549 |
TRG_NLS_MonoExtN_4 | 438 | 445 | PF00514 | 0.568 |
TRG_Pf-PMV_PEXEL_1 | 242 | 246 | PF00026 | 0.672 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7XAV9 | Leishmania donovani | 64% | 100% |
A4IDJ3 | Leishmania infantum | 64% | 100% |
E9ASZ6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 61% | 100% |
Q4Q1K2 | Leishmania major | 64% | 99% |