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: Q4QAN3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 172 | 176 | PF00656 | 0.701 |
CLV_NRD_NRD_1 | 178 | 180 | PF00675 | 0.731 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.650 |
CLV_NRD_NRD_1 | 343 | 345 | PF00675 | 0.787 |
CLV_NRD_NRD_1 | 416 | 418 | PF00675 | 0.593 |
CLV_NRD_NRD_1 | 423 | 425 | PF00675 | 0.568 |
CLV_PCSK_FUR_1 | 343 | 347 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 178 | 180 | PF00082 | 0.751 |
CLV_PCSK_KEX2_1 | 19 | 21 | PF00082 | 0.655 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.675 |
CLV_PCSK_KEX2_1 | 342 | 344 | PF00082 | 0.776 |
CLV_PCSK_KEX2_1 | 345 | 347 | PF00082 | 0.741 |
CLV_PCSK_KEX2_1 | 416 | 418 | PF00082 | 0.605 |
CLV_PCSK_KEX2_1 | 423 | 425 | PF00082 | 0.597 |
CLV_PCSK_PC1ET2_1 | 19 | 21 | PF00082 | 0.655 |
CLV_PCSK_PC1ET2_1 | 2 | 4 | PF00082 | 0.675 |
CLV_PCSK_PC1ET2_1 | 345 | 347 | PF00082 | 0.519 |
CLV_PCSK_SKI1_1 | 416 | 420 | PF00082 | 0.607 |
DEG_APCC_DBOX_1 | 3 | 11 | PF00400 | 0.624 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.670 |
DEG_SPOP_SBC_1 | 240 | 244 | PF00917 | 0.616 |
DEG_SPOP_SBC_1 | 450 | 454 | PF00917 | 0.646 |
DOC_ANK_TNKS_1 | 82 | 89 | PF00023 | 0.499 |
DOC_CDC14_PxL_1 | 260 | 268 | PF14671 | 0.674 |
DOC_MAPK_gen_1 | 2 | 10 | PF00069 | 0.654 |
DOC_MAPK_gen_1 | 250 | 259 | PF00069 | 0.572 |
DOC_PP2B_LxvP_1 | 401 | 404 | PF13499 | 0.686 |
DOC_USP7_MATH_1 | 145 | 149 | PF00917 | 0.769 |
DOC_USP7_MATH_1 | 169 | 173 | PF00917 | 0.749 |
DOC_USP7_MATH_1 | 218 | 222 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 280 | 284 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 288 | 292 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 310 | 314 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 450 | 454 | PF00917 | 0.731 |
DOC_USP7_MATH_1 | 492 | 496 | PF00917 | 0.757 |
DOC_USP7_MATH_1 | 54 | 58 | PF00917 | 0.520 |
DOC_WW_Pin1_4 | 114 | 119 | PF00397 | 0.666 |
DOC_WW_Pin1_4 | 146 | 151 | PF00397 | 0.674 |
DOC_WW_Pin1_4 | 266 | 271 | PF00397 | 0.660 |
DOC_WW_Pin1_4 | 286 | 291 | PF00397 | 0.490 |
DOC_WW_Pin1_4 | 88 | 93 | PF00397 | 0.669 |
LIG_14-3-3_CanoR_1 | 185 | 191 | PF00244 | 0.583 |
LIG_14-3-3_CanoR_1 | 481 | 491 | PF00244 | 0.586 |
LIG_BRCT_BRCA1_1 | 291 | 295 | PF00533 | 0.667 |
LIG_BRCT_BRCA1_1 | 436 | 440 | PF00533 | 0.540 |
LIG_BRCT_BRCA1_1 | 517 | 521 | PF00533 | 0.636 |
LIG_EVH1_1 | 401 | 405 | PF00568 | 0.679 |
LIG_EVH1_2 | 126 | 130 | PF00568 | 0.692 |
LIG_FHA_1 | 254 | 260 | PF00498 | 0.650 |
LIG_FHA_1 | 304 | 310 | PF00498 | 0.658 |
LIG_FHA_1 | 446 | 452 | PF00498 | 0.611 |
LIG_FHA_1 | 460 | 466 | PF00498 | 0.615 |
LIG_FHA_1 | 508 | 514 | PF00498 | 0.633 |
LIG_FHA_1 | 518 | 524 | PF00498 | 0.546 |
LIG_FHA_1 | 72 | 78 | PF00498 | 0.528 |
LIG_FHA_2 | 100 | 106 | PF00498 | 0.520 |
LIG_FHA_2 | 23 | 29 | PF00498 | 0.664 |
LIG_FHA_2 | 292 | 298 | PF00498 | 0.642 |
LIG_FHA_2 | 407 | 413 | PF00498 | 0.640 |
LIG_FHA_2 | 520 | 526 | PF00498 | 0.503 |
LIG_LIR_Gen_1 | 324 | 334 | PF02991 | 0.637 |
LIG_LIR_Nem_3 | 28 | 34 | PF02991 | 0.627 |
LIG_MYND_1 | 231 | 235 | PF01753 | 0.675 |
LIG_NRBOX | 105 | 111 | PF00104 | 0.568 |
LIG_PDZ_Class_1 | 543 | 548 | PF00595 | 0.500 |
LIG_PTB_Apo_2 | 157 | 164 | PF02174 | 0.691 |
LIG_PTB_Phospho_1 | 157 | 163 | PF10480 | 0.691 |
LIG_SH2_CRK | 260 | 264 | PF00017 | 0.682 |
LIG_SH2_PTP2 | 393 | 396 | PF00017 | 0.653 |
LIG_SH2_SRC | 393 | 396 | PF00017 | 0.653 |
LIG_SH2_STAT5 | 393 | 396 | PF00017 | 0.701 |
LIG_SH3_1 | 252 | 258 | PF00018 | 0.567 |
LIG_SH3_2 | 466 | 471 | PF14604 | 0.692 |
LIG_SH3_3 | 115 | 121 | PF00018 | 0.717 |
LIG_SH3_3 | 129 | 135 | PF00018 | 0.586 |
LIG_SH3_3 | 153 | 159 | PF00018 | 0.680 |
LIG_SH3_3 | 228 | 234 | PF00018 | 0.581 |
LIG_SH3_3 | 252 | 258 | PF00018 | 0.591 |
LIG_SH3_3 | 264 | 270 | PF00018 | 0.571 |
LIG_SH3_3 | 399 | 405 | PF00018 | 0.796 |
LIG_SH3_3 | 463 | 469 | PF00018 | 0.678 |
LIG_SUMO_SIM_anti_2 | 102 | 112 | PF11976 | 0.529 |
LIG_SUMO_SIM_par_1 | 6 | 12 | PF11976 | 0.634 |
LIG_TRFH_1 | 260 | 264 | PF08558 | 0.682 |
LIG_WW_3 | 182 | 186 | PF00397 | 0.674 |
LIG_WW_3 | 405 | 409 | PF00397 | 0.647 |
MOD_CDK_SPK_2 | 117 | 122 | PF00069 | 0.590 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.725 |
MOD_CK1_1 | 239 | 245 | PF00069 | 0.722 |
MOD_CK1_1 | 289 | 295 | PF00069 | 0.633 |
MOD_CK1_1 | 373 | 379 | PF00069 | 0.671 |
MOD_CK1_1 | 460 | 466 | PF00069 | 0.600 |
MOD_CK1_1 | 495 | 501 | PF00069 | 0.604 |
MOD_CK2_1 | 130 | 136 | PF00069 | 0.576 |
MOD_CK2_1 | 22 | 28 | PF00069 | 0.805 |
MOD_CK2_1 | 291 | 297 | PF00069 | 0.693 |
MOD_CK2_1 | 406 | 412 | PF00069 | 0.648 |
MOD_CK2_1 | 451 | 457 | PF00069 | 0.654 |
MOD_CK2_1 | 79 | 85 | PF00069 | 0.592 |
MOD_CK2_1 | 99 | 105 | PF00069 | 0.367 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.751 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.726 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.680 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.726 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.674 |
MOD_GlcNHglycan | 372 | 375 | PF01048 | 0.598 |
MOD_GlcNHglycan | 476 | 480 | PF01048 | 0.612 |
MOD_GlcNHglycan | 484 | 487 | PF01048 | 0.635 |
MOD_GlcNHglycan | 499 | 502 | PF01048 | 0.574 |
MOD_GlcNHglycan | 536 | 539 | PF01048 | 0.583 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.697 |
MOD_GSK3_1 | 236 | 243 | PF00069 | 0.707 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.589 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.565 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.592 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.580 |
MOD_GSK3_1 | 445 | 452 | PF00069 | 0.586 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.597 |
MOD_GSK3_1 | 475 | 482 | PF00069 | 0.530 |
MOD_GSK3_1 | 493 | 500 | PF00069 | 0.603 |
MOD_GSK3_1 | 507 | 514 | PF00069 | 0.552 |
MOD_GSK3_1 | 515 | 522 | PF00069 | 0.661 |
MOD_LATS_1 | 18 | 24 | PF00433 | 0.667 |
MOD_N-GLC_2 | 337 | 339 | PF02516 | 0.627 |
MOD_N-GLC_2 | 540 | 542 | PF02516 | 0.481 |
MOD_NEK2_1 | 236 | 241 | PF00069 | 0.674 |
MOD_NEK2_1 | 347 | 352 | PF00069 | 0.711 |
MOD_NEK2_1 | 451 | 456 | PF00069 | 0.654 |
MOD_NEK2_1 | 519 | 524 | PF00069 | 0.523 |
MOD_PIKK_1 | 183 | 189 | PF00454 | 0.723 |
MOD_PIKK_1 | 511 | 517 | PF00454 | 0.620 |
MOD_PIKK_1 | 71 | 77 | PF00454 | 0.554 |
MOD_PKA_2 | 79 | 85 | PF00069 | 0.465 |
MOD_Plk_1 | 460 | 466 | PF00069 | 0.542 |
MOD_Plk_1 | 515 | 521 | PF00069 | 0.601 |
MOD_Plk_4 | 186 | 192 | PF00069 | 0.613 |
MOD_Plk_4 | 258 | 264 | PF00069 | 0.651 |
MOD_Plk_4 | 273 | 279 | PF00069 | 0.635 |
MOD_Plk_4 | 451 | 457 | PF00069 | 0.598 |
MOD_ProDKin_1 | 114 | 120 | PF00069 | 0.671 |
MOD_ProDKin_1 | 146 | 152 | PF00069 | 0.674 |
MOD_ProDKin_1 | 266 | 272 | PF00069 | 0.662 |
MOD_ProDKin_1 | 286 | 292 | PF00069 | 0.490 |
MOD_ProDKin_1 | 88 | 94 | PF00069 | 0.663 |
MOD_SUMO_rev_2 | 411 | 415 | PF00179 | 0.483 |
TRG_DiLeu_BaEn_1 | 105 | 110 | PF01217 | 0.515 |
TRG_ENDOCYTIC_2 | 260 | 263 | PF00928 | 0.683 |
TRG_ENDOCYTIC_2 | 393 | 396 | PF00928 | 0.653 |
TRG_ER_diArg_1 | 341 | 344 | PF00400 | 0.656 |
TRG_ER_diArg_1 | 416 | 418 | PF00400 | 0.562 |
TRG_NLS_MonoExtN_4 | 342 | 348 | PF00514 | 0.519 |
TRG_NLS_MonoExtN_4 | 423 | 428 | PF00514 | 0.623 |
TRG_Pf-PMV_PEXEL_1 | 416 | 420 | PF00026 | 0.607 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IEV1 | Leishmania donovani | 88% | 100% |
A4HDF6 | Leishmania braziliensis | 59% | 100% |
E9AH58 | Leishmania infantum | 88% | 100% |
E9AWU1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |