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: A4I7A6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 315 | 319 | PF00656 | 0.501 |
CLV_NRD_NRD_1 | 143 | 145 | PF00675 | 0.572 |
CLV_NRD_NRD_1 | 17 | 19 | PF00675 | 0.719 |
CLV_NRD_NRD_1 | 198 | 200 | PF00675 | 0.628 |
CLV_NRD_NRD_1 | 425 | 427 | PF00675 | 0.694 |
CLV_NRD_NRD_1 | 436 | 438 | PF00675 | 0.672 |
CLV_NRD_NRD_1 | 45 | 47 | PF00675 | 0.549 |
CLV_NRD_NRD_1 | 455 | 457 | PF00675 | 0.733 |
CLV_NRD_NRD_1 | 61 | 63 | PF00675 | 0.416 |
CLV_PCSK_KEX2_1 | 143 | 145 | PF00082 | 0.632 |
CLV_PCSK_KEX2_1 | 164 | 166 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 17 | 19 | PF00082 | 0.743 |
CLV_PCSK_KEX2_1 | 200 | 202 | PF00082 | 0.585 |
CLV_PCSK_KEX2_1 | 212 | 214 | PF00082 | 0.559 |
CLV_PCSK_KEX2_1 | 325 | 327 | PF00082 | 0.675 |
CLV_PCSK_KEX2_1 | 425 | 427 | PF00082 | 0.661 |
CLV_PCSK_KEX2_1 | 436 | 438 | PF00082 | 0.613 |
CLV_PCSK_KEX2_1 | 45 | 47 | PF00082 | 0.542 |
CLV_PCSK_PC1ET2_1 | 164 | 166 | PF00082 | 0.526 |
CLV_PCSK_PC1ET2_1 | 200 | 202 | PF00082 | 0.585 |
CLV_PCSK_PC1ET2_1 | 212 | 214 | PF00082 | 0.446 |
CLV_PCSK_PC1ET2_1 | 325 | 327 | PF00082 | 0.625 |
CLV_PCSK_PC7_1 | 160 | 166 | PF00082 | 0.505 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.407 |
CLV_PCSK_SKI1_1 | 23 | 27 | PF00082 | 0.599 |
CLV_Separin_Metazoa | 157 | 161 | PF03568 | 0.521 |
DOC_CKS1_1 | 411 | 416 | PF01111 | 0.569 |
DOC_CKS1_1 | 452 | 457 | PF01111 | 0.660 |
DOC_MAPK_gen_1 | 425 | 433 | PF00069 | 0.601 |
DOC_MAPK_gen_1 | 45 | 53 | PF00069 | 0.402 |
DOC_MAPK_MEF2A_6 | 342 | 351 | PF00069 | 0.570 |
DOC_MAPK_MEF2A_6 | 45 | 53 | PF00069 | 0.402 |
DOC_PP1_RVXF_1 | 178 | 184 | PF00149 | 0.462 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.531 |
DOC_USP7_MATH_1 | 221 | 225 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 312 | 316 | PF00917 | 0.574 |
DOC_USP7_MATH_1 | 335 | 339 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 361 | 365 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 393 | 397 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 421 | 425 | PF00917 | 0.673 |
DOC_USP7_MATH_1 | 73 | 77 | PF00917 | 0.540 |
DOC_WW_Pin1_4 | 27 | 32 | PF00397 | 0.513 |
DOC_WW_Pin1_4 | 365 | 370 | PF00397 | 0.653 |
DOC_WW_Pin1_4 | 377 | 382 | PF00397 | 0.554 |
DOC_WW_Pin1_4 | 410 | 415 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 451 | 456 | PF00397 | 0.650 |
DOC_WW_Pin1_4 | 7 | 12 | PF00397 | 0.727 |
LIG_14-3-3_CanoR_1 | 296 | 304 | PF00244 | 0.473 |
LIG_14-3-3_CanoR_1 | 425 | 434 | PF00244 | 0.677 |
LIG_BRCT_BRCA1_1 | 429 | 433 | PF00533 | 0.636 |
LIG_deltaCOP1_diTrp_1 | 322 | 329 | PF00928 | 0.490 |
LIG_EVH1_1 | 410 | 414 | PF00568 | 0.564 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.568 |
LIG_FHA_1 | 27 | 33 | PF00498 | 0.601 |
LIG_FHA_1 | 339 | 345 | PF00498 | 0.595 |
LIG_FHA_1 | 350 | 356 | PF00498 | 0.460 |
LIG_FHA_2 | 117 | 123 | PF00498 | 0.512 |
LIG_FHA_2 | 193 | 199 | PF00498 | 0.473 |
LIG_FHA_2 | 36 | 42 | PF00498 | 0.558 |
LIG_FHA_2 | 430 | 436 | PF00498 | 0.571 |
LIG_LIR_Gen_1 | 224 | 233 | PF02991 | 0.565 |
LIG_LIR_Gen_1 | 446 | 455 | PF02991 | 0.639 |
LIG_LIR_Nem_3 | 224 | 229 | PF02991 | 0.606 |
LIG_LIR_Nem_3 | 37 | 42 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 446 | 452 | PF02991 | 0.632 |
LIG_Pex14_2 | 449 | 453 | PF04695 | 0.639 |
LIG_SH2_NCK_1 | 167 | 171 | PF00017 | 0.523 |
LIG_SH2_STAT5 | 173 | 176 | PF00017 | 0.577 |
LIG_SH2_STAT5 | 92 | 95 | PF00017 | 0.521 |
LIG_SH3_1 | 408 | 414 | PF00018 | 0.595 |
LIG_SH3_3 | 25 | 31 | PF00018 | 0.602 |
LIG_SH3_3 | 408 | 414 | PF00018 | 0.592 |
LIG_SH3_3 | 415 | 421 | PF00018 | 0.584 |
LIG_SH3_3 | 428 | 434 | PF00018 | 0.544 |
LIG_SH3_4 | 244 | 251 | PF00018 | 0.656 |
LIG_SUMO_SIM_par_1 | 345 | 350 | PF11976 | 0.539 |
LIG_SUMO_SIM_par_1 | 48 | 55 | PF11976 | 0.401 |
LIG_TRAF2_1 | 106 | 109 | PF00917 | 0.378 |
LIG_TRAF2_1 | 138 | 141 | PF00917 | 0.512 |
LIG_TRAF2_1 | 149 | 152 | PF00917 | 0.466 |
LIG_TRAF2_1 | 195 | 198 | PF00917 | 0.546 |
LIG_WRC_WIRS_1 | 36 | 41 | PF05994 | 0.511 |
MOD_CDK_SPK_2 | 451 | 456 | PF00069 | 0.650 |
MOD_CDK_SPxK_1 | 451 | 457 | PF00069 | 0.657 |
MOD_CDK_SPxxK_3 | 365 | 372 | PF00069 | 0.616 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.558 |
MOD_CK1_1 | 338 | 344 | PF00069 | 0.594 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.537 |
MOD_CK1_1 | 364 | 370 | PF00069 | 0.668 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.790 |
MOD_CK1_1 | 443 | 449 | PF00069 | 0.584 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.391 |
MOD_CK2_1 | 116 | 122 | PF00069 | 0.509 |
MOD_CK2_1 | 192 | 198 | PF00069 | 0.519 |
MOD_CK2_1 | 281 | 287 | PF00069 | 0.542 |
MOD_CK2_1 | 35 | 41 | PF00069 | 0.563 |
MOD_CK2_1 | 429 | 435 | PF00069 | 0.594 |
MOD_GlcNHglycan | 225 | 229 | PF01048 | 0.560 |
MOD_GlcNHglycan | 283 | 286 | PF01048 | 0.541 |
MOD_GlcNHglycan | 363 | 366 | PF01048 | 0.598 |
MOD_GlcNHglycan | 369 | 372 | PF01048 | 0.663 |
MOD_GlcNHglycan | 395 | 398 | PF01048 | 0.754 |
MOD_GlcNHglycan | 399 | 402 | PF01048 | 0.730 |
MOD_GlcNHglycan | 404 | 407 | PF01048 | 0.671 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.636 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.572 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.437 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.547 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.716 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.506 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.583 |
MOD_GSK3_1 | 361 | 368 | PF00069 | 0.574 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.749 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.698 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.586 |
MOD_N-GLC_1 | 26 | 31 | PF02516 | 0.579 |
MOD_N-GLC_1 | 393 | 398 | PF02516 | 0.648 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.517 |
MOD_NEK2_1 | 26 | 31 | PF00069 | 0.608 |
MOD_NEK2_1 | 268 | 273 | PF00069 | 0.616 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.573 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.542 |
MOD_NEK2_1 | 347 | 352 | PF00069 | 0.555 |
MOD_NEK2_2 | 448 | 453 | PF00069 | 0.635 |
MOD_PKA_1 | 425 | 431 | PF00069 | 0.627 |
MOD_PKA_2 | 231 | 237 | PF00069 | 0.625 |
MOD_PKA_2 | 295 | 301 | PF00069 | 0.567 |
MOD_PKA_2 | 425 | 431 | PF00069 | 0.687 |
MOD_Plk_1 | 224 | 230 | PF00069 | 0.586 |
MOD_Plk_1 | 347 | 353 | PF00069 | 0.552 |
MOD_Plk_2-3 | 429 | 435 | PF00069 | 0.576 |
MOD_Plk_4 | 448 | 454 | PF00069 | 0.637 |
MOD_ProDKin_1 | 27 | 33 | PF00069 | 0.510 |
MOD_ProDKin_1 | 365 | 371 | PF00069 | 0.656 |
MOD_ProDKin_1 | 377 | 383 | PF00069 | 0.552 |
MOD_ProDKin_1 | 410 | 416 | PF00069 | 0.637 |
MOD_ProDKin_1 | 451 | 457 | PF00069 | 0.657 |
MOD_ProDKin_1 | 7 | 13 | PF00069 | 0.724 |
MOD_SUMO_for_1 | 106 | 109 | PF00179 | 0.490 |
MOD_SUMO_for_1 | 179 | 182 | PF00179 | 0.509 |
MOD_SUMO_rev_2 | 109 | 117 | PF00179 | 0.560 |
TRG_DiLeu_BaEn_1 | 300 | 305 | PF01217 | 0.453 |
TRG_DiLeu_BaLyEn_6 | 434 | 439 | PF01217 | 0.663 |
TRG_ENDOCYTIC_2 | 156 | 159 | PF00928 | 0.553 |
TRG_ENDOCYTIC_2 | 167 | 170 | PF00928 | 0.528 |
TRG_ER_diArg_1 | 16 | 18 | PF00400 | 0.619 |
TRG_ER_diArg_1 | 199 | 202 | PF00400 | 0.623 |
TRG_ER_diArg_1 | 436 | 438 | PF00400 | 0.655 |
TRG_Pf-PMV_PEXEL_1 | 207 | 211 | PF00026 | 0.419 |
TRG_Pf-PMV_PEXEL_1 | 259 | 264 | PF00026 | 0.453 |
TRG_Pf-PMV_PEXEL_1 | 436 | 440 | PF00026 | 0.659 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7X505 | Leishmania donovani | 98% | 88% |
A4HJU0 | Leishmania braziliensis | 60% | 100% |
E9B2A0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
Q4Q5V7 | Leishmania major | 86% | 100% |