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: 2, no: 4 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: Q4QHT6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 241 | 245 | PF00656 | 0.442 |
CLV_NRD_NRD_1 | 159 | 161 | PF00675 | 0.789 |
CLV_NRD_NRD_1 | 170 | 172 | PF00675 | 0.518 |
CLV_NRD_NRD_1 | 178 | 180 | PF00675 | 0.360 |
CLV_NRD_NRD_1 | 247 | 249 | PF00675 | 0.462 |
CLV_NRD_NRD_1 | 435 | 437 | PF00675 | 0.682 |
CLV_NRD_NRD_1 | 466 | 468 | PF00675 | 0.702 |
CLV_PCSK_KEX2_1 | 159 | 161 | PF00082 | 0.789 |
CLV_PCSK_KEX2_1 | 170 | 172 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 178 | 180 | PF00082 | 0.360 |
CLV_PCSK_KEX2_1 | 247 | 249 | PF00082 | 0.462 |
CLV_PCSK_KEX2_1 | 368 | 370 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 391 | 393 | PF00082 | 0.569 |
CLV_PCSK_KEX2_1 | 473 | 475 | PF00082 | 0.629 |
CLV_PCSK_KEX2_1 | 479 | 481 | PF00082 | 0.576 |
CLV_PCSK_PC1ET2_1 | 368 | 370 | PF00082 | 0.614 |
CLV_PCSK_PC1ET2_1 | 391 | 393 | PF00082 | 0.542 |
CLV_PCSK_PC1ET2_1 | 473 | 475 | PF00082 | 0.629 |
CLV_PCSK_PC1ET2_1 | 479 | 481 | PF00082 | 0.576 |
CLV_PCSK_SKI1_1 | 3 | 7 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 392 | 396 | PF00082 | 0.574 |
CLV_PCSK_SKI1_1 | 436 | 440 | PF00082 | 0.683 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.551 |
DEG_SCF_FBW7_1 | 359 | 365 | PF00400 | 0.548 |
DOC_CKS1_1 | 359 | 364 | PF01111 | 0.550 |
DOC_CYCLIN_yCln2_LP_2 | 297 | 303 | PF00134 | 0.621 |
DOC_PP2B_LxvP_1 | 297 | 300 | PF13499 | 0.616 |
DOC_USP7_MATH_1 | 123 | 127 | PF00917 | 0.634 |
DOC_USP7_MATH_1 | 271 | 275 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 362 | 366 | PF00917 | 0.686 |
DOC_USP7_MATH_1 | 39 | 43 | PF00917 | 0.629 |
DOC_USP7_MATH_1 | 462 | 466 | PF00917 | 0.765 |
DOC_USP7_UBL2_3 | 314 | 318 | PF12436 | 0.606 |
DOC_USP7_UBL2_3 | 391 | 395 | PF12436 | 0.629 |
DOC_USP7_UBL2_3 | 424 | 428 | PF12436 | 0.614 |
DOC_USP7_UBL2_3 | 433 | 437 | PF12436 | 0.633 |
DOC_USP7_UBL2_3 | 440 | 444 | PF12436 | 0.577 |
DOC_USP7_UBL2_3 | 468 | 472 | PF12436 | 0.627 |
DOC_WW_Pin1_4 | 153 | 158 | PF00397 | 0.533 |
DOC_WW_Pin1_4 | 195 | 200 | PF00397 | 0.481 |
DOC_WW_Pin1_4 | 348 | 353 | PF00397 | 0.587 |
DOC_WW_Pin1_4 | 358 | 363 | PF00397 | 0.616 |
DOC_WW_Pin1_4 | 405 | 410 | PF00397 | 0.640 |
LIG_14-3-3_CanoR_1 | 122 | 128 | PF00244 | 0.521 |
LIG_14-3-3_CanoR_1 | 321 | 329 | PF00244 | 0.657 |
LIG_14-3-3_CanoR_1 | 446 | 454 | PF00244 | 0.673 |
LIG_14-3-3_CanoR_1 | 467 | 475 | PF00244 | 0.629 |
LIG_Actin_WH2_2 | 322 | 339 | PF00022 | 0.513 |
LIG_BIR_III_4 | 68 | 72 | PF00653 | 0.555 |
LIG_Clathr_ClatBox_1 | 82 | 86 | PF01394 | 0.621 |
LIG_FHA_1 | 199 | 205 | PF00498 | 0.466 |
LIG_FHA_2 | 236 | 242 | PF00498 | 0.605 |
LIG_FHA_2 | 288 | 294 | PF00498 | 0.681 |
LIG_LIR_Nem_3 | 93 | 99 | PF02991 | 0.540 |
LIG_NRP_CendR_1 | 483 | 484 | PF00754 | 0.689 |
LIG_Pex14_2 | 100 | 104 | PF04695 | 0.527 |
LIG_SH2_NCK_1 | 338 | 342 | PF00017 | 0.528 |
LIG_SH2_STAP1 | 338 | 342 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 96 | 99 | PF00017 | 0.544 |
LIG_SH3_1 | 395 | 401 | PF00018 | 0.603 |
LIG_SH3_2 | 398 | 403 | PF14604 | 0.612 |
LIG_SH3_3 | 193 | 199 | PF00018 | 0.491 |
LIG_SH3_3 | 356 | 362 | PF00018 | 0.645 |
LIG_SH3_3 | 395 | 401 | PF00018 | 0.571 |
LIG_SH3_3 | 439 | 445 | PF00018 | 0.643 |
LIG_SH3_4 | 433 | 440 | PF00018 | 0.691 |
LIG_SUMO_SIM_anti_2 | 111 | 118 | PF11976 | 0.591 |
LIG_SUMO_SIM_par_1 | 81 | 88 | PF11976 | 0.616 |
LIG_WW_3 | 433 | 437 | PF00397 | 0.554 |
MOD_CDC14_SPxK_1 | 156 | 159 | PF00782 | 0.530 |
MOD_CDK_SPK_2 | 348 | 353 | PF00069 | 0.630 |
MOD_CDK_SPxK_1 | 153 | 159 | PF00069 | 0.532 |
MOD_CDK_SPxxK_3 | 153 | 160 | PF00069 | 0.531 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.645 |
MOD_CK1_1 | 18 | 24 | PF00069 | 0.573 |
MOD_CK1_1 | 184 | 190 | PF00069 | 0.535 |
MOD_CK1_1 | 195 | 201 | PF00069 | 0.438 |
MOD_CK1_1 | 276 | 282 | PF00069 | 0.632 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.657 |
MOD_CK2_1 | 235 | 241 | PF00069 | 0.470 |
MOD_CK2_1 | 287 | 293 | PF00069 | 0.677 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.685 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.528 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.646 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.601 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.645 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.578 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.556 |
MOD_GlcNHglycan | 41 | 44 | PF01048 | 0.391 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.567 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.557 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.603 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.504 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.655 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.605 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.654 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.640 |
MOD_GSK3_1 | 446 | 453 | PF00069 | 0.543 |
MOD_GSK3_1 | 462 | 469 | PF00069 | 0.573 |
MOD_N-GLC_1 | 219 | 224 | PF02516 | 0.437 |
MOD_N-GLC_1 | 348 | 353 | PF02516 | 0.619 |
MOD_N-GLC_1 | 88 | 93 | PF02516 | 0.589 |
MOD_NEK2_1 | 16 | 21 | PF00069 | 0.678 |
MOD_NEK2_1 | 203 | 208 | PF00069 | 0.494 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.472 |
MOD_NEK2_1 | 336 | 341 | PF00069 | 0.517 |
MOD_NEK2_1 | 49 | 54 | PF00069 | 0.603 |
MOD_NEK2_2 | 58 | 63 | PF00069 | 0.692 |
MOD_PIKK_1 | 184 | 190 | PF00454 | 0.467 |
MOD_PIKK_1 | 203 | 209 | PF00454 | 0.447 |
MOD_PIKK_1 | 265 | 271 | PF00454 | 0.692 |
MOD_PIKK_1 | 273 | 279 | PF00454 | 0.457 |
MOD_PIKK_1 | 49 | 55 | PF00454 | 0.634 |
MOD_PIKK_1 | 61 | 67 | PF00454 | 0.646 |
MOD_PK_1 | 450 | 456 | PF00069 | 0.644 |
MOD_PKA_1 | 368 | 374 | PF00069 | 0.636 |
MOD_PKA_1 | 436 | 442 | PF00069 | 0.683 |
MOD_PKA_2 | 320 | 326 | PF00069 | 0.660 |
MOD_PKA_2 | 336 | 342 | PF00069 | 0.508 |
MOD_PKA_2 | 368 | 374 | PF00069 | 0.654 |
MOD_PKA_2 | 445 | 451 | PF00069 | 0.651 |
MOD_PKA_2 | 466 | 472 | PF00069 | 0.695 |
MOD_PKA_2 | 6 | 12 | PF00069 | 0.611 |
MOD_PKB_1 | 179 | 187 | PF00069 | 0.533 |
MOD_Plk_1 | 110 | 116 | PF00069 | 0.635 |
MOD_Plk_1 | 140 | 146 | PF00069 | 0.659 |
MOD_Plk_1 | 219 | 225 | PF00069 | 0.429 |
MOD_Plk_1 | 31 | 37 | PF00069 | 0.482 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.635 |
MOD_Plk_4 | 287 | 293 | PF00069 | 0.629 |
MOD_Plk_4 | 325 | 331 | PF00069 | 0.567 |
MOD_ProDKin_1 | 153 | 159 | PF00069 | 0.532 |
MOD_ProDKin_1 | 195 | 201 | PF00069 | 0.476 |
MOD_ProDKin_1 | 348 | 354 | PF00069 | 0.592 |
MOD_ProDKin_1 | 358 | 364 | PF00069 | 0.619 |
MOD_ProDKin_1 | 405 | 411 | PF00069 | 0.637 |
MOD_SUMO_for_1 | 226 | 229 | PF00179 | 0.429 |
TRG_ER_diArg_1 | 170 | 172 | PF00400 | 0.570 |
TRG_ER_diArg_1 | 178 | 181 | PF00400 | 0.424 |
TRG_ER_diArg_1 | 246 | 248 | PF00400 | 0.479 |
TRG_ER_diArg_1 | 474 | 477 | PF00400 | 0.542 |
TRG_NLS_MonoCore_2 | 472 | 477 | PF00514 | 0.542 |
TRG_NLS_MonoExtC_3 | 471 | 476 | PF00514 | 0.543 |
TRG_NLS_MonoExtN_4 | 472 | 477 | PF00514 | 0.560 |
TRG_Pf-PMV_PEXEL_1 | 107 | 111 | PF00026 | 0.572 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ILW1 | Leptomonas seymouri | 44% | 94% |
A0A3Q8I7H5 | Leishmania donovani | 89% | 99% |
A4H5N7 | Leishmania braziliensis | 58% | 98% |
A4HU09 | Leishmania infantum | 89% | 99% |
E9AMT9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 94% |