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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: E9B2V2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 437 | 441 | PF00656 | 0.654 |
CLV_C14_Caspase3-7 | 455 | 459 | PF00656 | 0.491 |
CLV_NRD_NRD_1 | 205 | 207 | PF00675 | 0.627 |
CLV_NRD_NRD_1 | 306 | 308 | PF00675 | 0.439 |
CLV_NRD_NRD_1 | 351 | 353 | PF00675 | 0.505 |
CLV_PCSK_FUR_1 | 304 | 308 | PF00082 | 0.370 |
CLV_PCSK_FUR_1 | 352 | 356 | PF00082 | 0.569 |
CLV_PCSK_KEX2_1 | 118 | 120 | PF00082 | 0.487 |
CLV_PCSK_KEX2_1 | 205 | 207 | PF00082 | 0.627 |
CLV_PCSK_KEX2_1 | 306 | 308 | PF00082 | 0.439 |
CLV_PCSK_KEX2_1 | 354 | 356 | PF00082 | 0.570 |
CLV_PCSK_KEX2_1 | 491 | 493 | PF00082 | 0.517 |
CLV_PCSK_PC1ET2_1 | 118 | 120 | PF00082 | 0.462 |
CLV_PCSK_PC1ET2_1 | 354 | 356 | PF00082 | 0.570 |
CLV_PCSK_PC1ET2_1 | 491 | 493 | PF00082 | 0.517 |
CLV_PCSK_PC7_1 | 114 | 120 | PF00082 | 0.460 |
CLV_PCSK_PC7_1 | 350 | 356 | PF00082 | 0.565 |
CLV_PCSK_SKI1_1 | 217 | 221 | PF00082 | 0.695 |
CLV_PCSK_SKI1_1 | 371 | 375 | PF00082 | 0.637 |
CLV_PCSK_SKI1_1 | 471 | 475 | PF00082 | 0.593 |
DEG_APCC_DBOX_1 | 233 | 241 | PF00400 | 0.590 |
DEG_APCC_KENBOX_2 | 180 | 184 | PF00400 | 0.424 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.592 |
DEG_SPOP_SBC_1 | 431 | 435 | PF00917 | 0.655 |
DOC_ANK_TNKS_1 | 335 | 342 | PF00023 | 0.445 |
DOC_CYCLIN_yCln2_LP_2 | 29 | 35 | PF00134 | 0.450 |
DOC_MAPK_gen_1 | 23 | 31 | PF00069 | 0.456 |
DOC_MAPK_gen_1 | 304 | 312 | PF00069 | 0.391 |
DOC_MAPK_gen_1 | 376 | 385 | PF00069 | 0.524 |
DOC_MAPK_MEF2A_6 | 142 | 151 | PF00069 | 0.430 |
DOC_PP2B_LxvP_1 | 383 | 386 | PF13499 | 0.490 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.597 |
DOC_USP7_MATH_1 | 24 | 28 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 388 | 392 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 431 | 435 | PF00917 | 0.680 |
DOC_USP7_UBL2_3 | 370 | 374 | PF12436 | 0.557 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.635 |
DOC_WW_Pin1_4 | 427 | 432 | PF00397 | 0.673 |
DOC_WW_Pin1_4 | 440 | 445 | PF00397 | 0.588 |
LIG_14-3-3_CanoR_1 | 200 | 204 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 248 | 257 | PF00244 | 0.559 |
LIG_14-3-3_CanoR_1 | 366 | 373 | PF00244 | 0.422 |
LIG_14-3-3_CanoR_1 | 432 | 442 | PF00244 | 0.608 |
LIG_Actin_WH2_2 | 457 | 473 | PF00022 | 0.522 |
LIG_APCC_ABBA_1 | 136 | 141 | PF00400 | 0.438 |
LIG_BIR_III_2 | 410 | 414 | PF00653 | 0.506 |
LIG_BRCT_BRCA1_1 | 27 | 31 | PF00533 | 0.629 |
LIG_Clathr_ClatBox_1 | 146 | 150 | PF01394 | 0.481 |
LIG_EH1_1 | 30 | 38 | PF00400 | 0.582 |
LIG_FHA_1 | 11 | 17 | PF00498 | 0.477 |
LIG_FHA_1 | 249 | 255 | PF00498 | 0.537 |
LIG_FHA_1 | 273 | 279 | PF00498 | 0.675 |
LIG_FHA_1 | 472 | 478 | PF00498 | 0.581 |
LIG_FHA_1 | 87 | 93 | PF00498 | 0.378 |
LIG_FHA_2 | 333 | 339 | PF00498 | 0.410 |
LIG_FHA_2 | 405 | 411 | PF00498 | 0.530 |
LIG_FHA_2 | 435 | 441 | PF00498 | 0.656 |
LIG_FHA_2 | 453 | 459 | PF00498 | 0.616 |
LIG_FHA_2 | 476 | 482 | PF00498 | 0.548 |
LIG_LIR_Gen_1 | 150 | 159 | PF02991 | 0.489 |
LIG_LIR_Gen_1 | 297 | 308 | PF02991 | 0.480 |
LIG_LIR_Gen_1 | 466 | 477 | PF02991 | 0.643 |
LIG_LIR_Gen_1 | 54 | 64 | PF02991 | 0.523 |
LIG_LIR_Gen_1 | 85 | 96 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 150 | 154 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 297 | 303 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 440 | 445 | PF02991 | 0.581 |
LIG_LIR_Nem_3 | 466 | 472 | PF02991 | 0.647 |
LIG_LIR_Nem_3 | 54 | 60 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 85 | 91 | PF02991 | 0.487 |
LIG_NRBOX | 236 | 242 | PF00104 | 0.642 |
LIG_Pex14_2 | 57 | 61 | PF04695 | 0.525 |
LIG_SH2_NCK_1 | 162 | 166 | PF00017 | 0.322 |
LIG_SH2_STAP1 | 162 | 166 | PF00017 | 0.322 |
LIG_SH2_STAT3 | 236 | 239 | PF00017 | 0.583 |
LIG_SH2_STAT3 | 343 | 346 | PF00017 | 0.541 |
LIG_SH2_STAT5 | 236 | 239 | PF00017 | 0.507 |
LIG_SH2_STAT5 | 469 | 472 | PF00017 | 0.598 |
LIG_SH3_3 | 382 | 388 | PF00018 | 0.513 |
LIG_Sin3_3 | 109 | 116 | PF02671 | 0.530 |
LIG_SUMO_SIM_par_1 | 145 | 150 | PF11976 | 0.378 |
LIG_SUMO_SIM_par_1 | 255 | 260 | PF11976 | 0.539 |
LIG_SUMO_SIM_par_1 | 308 | 314 | PF11976 | 0.420 |
LIG_TRAF2_1 | 194 | 197 | PF00917 | 0.400 |
LIG_TRAF2_1 | 344 | 347 | PF00917 | 0.637 |
LIG_TRAF2_1 | 71 | 74 | PF00917 | 0.517 |
LIG_TRAF2_1 | 82 | 85 | PF00917 | 0.369 |
LIG_TYR_ITIM | 467 | 472 | PF00017 | 0.527 |
LIG_UBA3_1 | 126 | 132 | PF00899 | 0.512 |
MOD_CDK_SPK_2 | 427 | 432 | PF00069 | 0.584 |
MOD_CDK_SPxxK_3 | 440 | 447 | PF00069 | 0.508 |
MOD_CK1_1 | 199 | 205 | PF00069 | 0.526 |
MOD_CK1_1 | 244 | 250 | PF00069 | 0.653 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.485 |
MOD_CK1_1 | 400 | 406 | PF00069 | 0.635 |
MOD_CK1_1 | 430 | 436 | PF00069 | 0.645 |
MOD_CK1_1 | 443 | 449 | PF00069 | 0.586 |
MOD_CK2_1 | 332 | 338 | PF00069 | 0.413 |
MOD_CK2_1 | 475 | 481 | PF00069 | 0.496 |
MOD_CK2_1 | 68 | 74 | PF00069 | 0.523 |
MOD_Cter_Amidation | 304 | 307 | PF01082 | 0.349 |
MOD_GlcNHglycan | 356 | 360 | PF01048 | 0.521 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.500 |
MOD_GlcNHglycan | 402 | 405 | PF01048 | 0.533 |
MOD_GlcNHglycan | 486 | 489 | PF01048 | 0.534 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.634 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.599 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.432 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.585 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.686 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.667 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.730 |
MOD_GSK3_1 | 427 | 434 | PF00069 | 0.640 |
MOD_GSK3_1 | 471 | 478 | PF00069 | 0.584 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.475 |
MOD_N-GLC_1 | 440 | 445 | PF02516 | 0.577 |
MOD_NEK2_1 | 201 | 206 | PF00069 | 0.510 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.644 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.578 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.506 |
MOD_NEK2_1 | 272 | 277 | PF00069 | 0.701 |
MOD_NEK2_1 | 332 | 337 | PF00069 | 0.398 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.482 |
MOD_PIKK_1 | 365 | 371 | PF00454 | 0.426 |
MOD_PKA_1 | 205 | 211 | PF00069 | 0.607 |
MOD_PKA_2 | 199 | 205 | PF00069 | 0.527 |
MOD_PKA_2 | 225 | 231 | PF00069 | 0.578 |
MOD_PKA_2 | 247 | 253 | PF00069 | 0.662 |
MOD_PKA_2 | 365 | 371 | PF00069 | 0.426 |
MOD_PKA_2 | 431 | 437 | PF00069 | 0.637 |
MOD_Plk_1 | 196 | 202 | PF00069 | 0.573 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.636 |
MOD_ProDKin_1 | 427 | 433 | PF00069 | 0.674 |
MOD_ProDKin_1 | 440 | 446 | PF00069 | 0.587 |
MOD_SUMO_for_1 | 490 | 493 | PF00179 | 0.465 |
TRG_DiLeu_BaEn_1 | 107 | 112 | PF01217 | 0.515 |
TRG_DiLeu_BaEn_1 | 150 | 155 | PF01217 | 0.491 |
TRG_DiLeu_BaEn_3 | 121 | 127 | PF01217 | 0.411 |
TRG_DiLeu_BaEn_4 | 168 | 174 | PF01217 | 0.378 |
TRG_DiLeu_BaEn_4 | 196 | 202 | PF01217 | 0.391 |
TRG_DiLeu_BaLyEn_6 | 267 | 272 | PF01217 | 0.543 |
TRG_DiLeu_BaLyEn_6 | 373 | 378 | PF01217 | 0.528 |
TRG_ENDOCYTIC_2 | 162 | 165 | PF00928 | 0.321 |
TRG_ENDOCYTIC_2 | 300 | 303 | PF00928 | 0.594 |
TRG_ENDOCYTIC_2 | 469 | 472 | PF00928 | 0.598 |
TRG_ER_diArg_1 | 289 | 292 | PF00400 | 0.460 |
TRG_ER_diArg_1 | 303 | 306 | PF00400 | 0.450 |
TRG_ER_diArg_1 | 378 | 381 | PF00400 | 0.636 |
TRG_NES_CRM1_1 | 124 | 140 | PF08389 | 0.454 |
TRG_Pf-PMV_PEXEL_1 | 376 | 380 | PF00026 | 0.489 |
TRG_Pf-PMV_PEXEL_1 | 447 | 451 | PF00026 | 0.507 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMW1 | Leptomonas seymouri | 44% | 85% |
A0A3Q8IG72 | Leishmania donovani | 83% | 100% |
A4HKG3 | Leishmania braziliensis | 62% | 100% |
A4I7Z1 | Leishmania infantum | 83% | 100% |
Q4Q5A4 | Leishmania major | 81% | 99% |