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: E9B3C9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 192 | 194 | PF00675 | 0.732 |
CLV_NRD_NRD_1 | 218 | 220 | PF00675 | 0.646 |
CLV_NRD_NRD_1 | 473 | 475 | PF00675 | 0.389 |
CLV_NRD_NRD_1 | 497 | 499 | PF00675 | 0.568 |
CLV_NRD_NRD_1 | 515 | 517 | PF00675 | 0.692 |
CLV_PCSK_KEX2_1 | 192 | 194 | PF00082 | 0.732 |
CLV_PCSK_KEX2_1 | 50 | 52 | PF00082 | 0.553 |
CLV_PCSK_KEX2_1 | 515 | 517 | PF00082 | 0.756 |
CLV_PCSK_PC1ET2_1 | 50 | 52 | PF00082 | 0.547 |
CLV_PCSK_SKI1_1 | 140 | 144 | PF00082 | 0.352 |
CLV_PCSK_SKI1_1 | 158 | 162 | PF00082 | 0.573 |
CLV_PCSK_SKI1_1 | 3 | 7 | PF00082 | 0.499 |
CLV_PCSK_SKI1_1 | 328 | 332 | PF00082 | 0.700 |
CLV_PCSK_SKI1_1 | 474 | 478 | PF00082 | 0.381 |
CLV_PCSK_SKI1_1 | 515 | 519 | PF00082 | 0.648 |
CLV_PCSK_SKI1_1 | 63 | 67 | PF00082 | 0.474 |
CLV_PCSK_SKI1_1 | 75 | 79 | PF00082 | 0.593 |
DEG_SCF_FBW7_1 | 339 | 346 | PF00400 | 0.528 |
DEG_SPOP_SBC_1 | 173 | 177 | PF00917 | 0.587 |
DEG_SPOP_SBC_1 | 179 | 183 | PF00917 | 0.644 |
DOC_CKS1_1 | 340 | 345 | PF01111 | 0.526 |
DOC_MAPK_gen_1 | 498 | 505 | PF00069 | 0.592 |
DOC_MAPK_HePTP_8 | 278 | 290 | PF00069 | 0.506 |
DOC_MAPK_MEF2A_6 | 281 | 290 | PF00069 | 0.684 |
DOC_MAPK_RevD_3 | 503 | 516 | PF00069 | 0.579 |
DOC_PP1_RVXF_1 | 305 | 311 | PF00149 | 0.709 |
DOC_PP1_RVXF_1 | 49 | 56 | PF00149 | 0.432 |
DOC_USP7_MATH_1 | 111 | 115 | PF00917 | 0.414 |
DOC_USP7_MATH_1 | 352 | 356 | PF00917 | 0.730 |
DOC_USP7_MATH_1 | 402 | 406 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 525 | 529 | PF00917 | 0.625 |
DOC_USP7_UBL2_3 | 9 | 13 | PF12436 | 0.733 |
DOC_WW_Pin1_4 | 130 | 135 | PF00397 | 0.389 |
DOC_WW_Pin1_4 | 182 | 187 | PF00397 | 0.564 |
DOC_WW_Pin1_4 | 296 | 301 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 339 | 344 | PF00397 | 0.681 |
DOC_WW_Pin1_4 | 381 | 386 | PF00397 | 0.669 |
DOC_WW_Pin1_4 | 510 | 515 | PF00397 | 0.807 |
DOC_WW_Pin1_4 | 517 | 522 | PF00397 | 0.662 |
DOC_WW_Pin1_4 | 66 | 71 | PF00397 | 0.479 |
LIG_14-3-3_CanoR_1 | 109 | 119 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 301 | 310 | PF00244 | 0.671 |
LIG_14-3-3_CanoR_1 | 434 | 442 | PF00244 | 0.577 |
LIG_14-3-3_CanoR_1 | 459 | 468 | PF00244 | 0.560 |
LIG_BIR_III_4 | 392 | 396 | PF00653 | 0.703 |
LIG_BRCT_BRCA1_1 | 227 | 231 | PF00533 | 0.523 |
LIG_FHA_1 | 259 | 265 | PF00498 | 0.711 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.396 |
LIG_FHA_1 | 500 | 506 | PF00498 | 0.632 |
LIG_FHA_1 | 507 | 513 | PF00498 | 0.637 |
LIG_FHA_2 | 312 | 318 | PF00498 | 0.685 |
LIG_FHA_2 | 367 | 373 | PF00498 | 0.695 |
LIG_FHA_2 | 460 | 466 | PF00498 | 0.572 |
LIG_GSK3_LRP6_1 | 339 | 344 | PF00069 | 0.527 |
LIG_Integrin_RGD_1 | 57 | 59 | PF01839 | 0.455 |
LIG_LIR_Gen_1 | 309 | 318 | PF02991 | 0.692 |
LIG_LIR_Nem_3 | 361 | 365 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 446 | 451 | PF02991 | 0.563 |
LIG_SH2_CRK | 119 | 123 | PF00017 | 0.446 |
LIG_SH2_CRK | 362 | 366 | PF00017 | 0.517 |
LIG_SH2_NCK_1 | 362 | 366 | PF00017 | 0.517 |
LIG_SH2_NCK_1 | 96 | 100 | PF00017 | 0.560 |
LIG_SH2_SRC | 362 | 365 | PF00017 | 0.516 |
LIG_SH2_STAT5 | 29 | 32 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 471 | 474 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 48 | 51 | PF00017 | 0.543 |
LIG_SH3_1 | 518 | 524 | PF00018 | 0.629 |
LIG_SH3_3 | 167 | 173 | PF00018 | 0.660 |
LIG_SH3_3 | 263 | 269 | PF00018 | 0.660 |
LIG_SH3_3 | 294 | 300 | PF00018 | 0.649 |
LIG_SH3_3 | 323 | 329 | PF00018 | 0.649 |
LIG_SH3_3 | 333 | 339 | PF00018 | 0.661 |
LIG_SH3_3 | 501 | 507 | PF00018 | 0.780 |
LIG_SH3_3 | 518 | 524 | PF00018 | 0.527 |
LIG_SH3_3 | 64 | 70 | PF00018 | 0.471 |
LIG_SH3_4 | 9 | 16 | PF00018 | 0.634 |
LIG_SUMO_SIM_anti_2 | 282 | 289 | PF11976 | 0.683 |
LIG_SUMO_SIM_par_1 | 285 | 291 | PF11976 | 0.634 |
LIG_UBA3_1 | 147 | 155 | PF00899 | 0.214 |
MOD_CDK_SPK_2 | 296 | 301 | PF00069 | 0.622 |
MOD_CDK_SPK_2 | 510 | 515 | PF00069 | 0.822 |
MOD_CDK_SPK_2 | 66 | 71 | PF00069 | 0.533 |
MOD_CDK_SPxK_1 | 510 | 516 | PF00069 | 0.746 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.648 |
MOD_CK1_1 | 222 | 228 | PF00069 | 0.818 |
MOD_CK1_1 | 366 | 372 | PF00069 | 0.796 |
MOD_CK1_1 | 528 | 534 | PF00069 | 0.637 |
MOD_CK2_1 | 366 | 372 | PF00069 | 0.519 |
MOD_CK2_1 | 66 | 72 | PF00069 | 0.458 |
MOD_Cter_Amidation | 190 | 193 | PF01082 | 0.510 |
MOD_Cter_Amidation | 472 | 475 | PF01082 | 0.389 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.703 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.735 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.547 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.730 |
MOD_GlcNHglycan | 354 | 357 | PF01048 | 0.641 |
MOD_GlcNHglycan | 435 | 438 | PF01048 | 0.611 |
MOD_GlcNHglycan | 527 | 530 | PF01048 | 0.700 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.718 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.772 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.741 |
MOD_GSK3_1 | 254 | 261 | PF00069 | 0.571 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.799 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.676 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.602 |
MOD_GSK3_1 | 506 | 513 | PF00069 | 0.756 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.499 |
MOD_LATS_1 | 447 | 453 | PF00433 | 0.437 |
MOD_N-GLC_1 | 127 | 132 | PF02516 | 0.517 |
MOD_N-GLC_1 | 244 | 249 | PF02516 | 0.715 |
MOD_N-GLC_1 | 352 | 357 | PF02516 | 0.738 |
MOD_N-GLC_1 | 443 | 448 | PF02516 | 0.576 |
MOD_N-GLC_1 | 449 | 454 | PF02516 | 0.558 |
MOD_NEK2_1 | 127 | 132 | PF00069 | 0.517 |
MOD_NEK2_1 | 320 | 325 | PF00069 | 0.661 |
MOD_NEK2_1 | 374 | 379 | PF00069 | 0.548 |
MOD_PIKK_1 | 363 | 369 | PF00454 | 0.689 |
MOD_PIKK_1 | 374 | 380 | PF00454 | 0.490 |
MOD_PKA_1 | 219 | 225 | PF00069 | 0.605 |
MOD_PKA_2 | 306 | 312 | PF00069 | 0.648 |
MOD_PKA_2 | 433 | 439 | PF00069 | 0.583 |
MOD_PKA_2 | 458 | 464 | PF00069 | 0.594 |
MOD_PKA_2 | 505 | 511 | PF00069 | 0.572 |
MOD_Plk_1 | 127 | 133 | PF00069 | 0.466 |
MOD_Plk_1 | 402 | 408 | PF00069 | 0.605 |
MOD_Plk_1 | 443 | 449 | PF00069 | 0.577 |
MOD_Plk_4 | 306 | 312 | PF00069 | 0.781 |
MOD_ProDKin_1 | 130 | 136 | PF00069 | 0.389 |
MOD_ProDKin_1 | 182 | 188 | PF00069 | 0.559 |
MOD_ProDKin_1 | 296 | 302 | PF00069 | 0.646 |
MOD_ProDKin_1 | 339 | 345 | PF00069 | 0.677 |
MOD_ProDKin_1 | 381 | 387 | PF00069 | 0.668 |
MOD_ProDKin_1 | 510 | 516 | PF00069 | 0.810 |
MOD_ProDKin_1 | 517 | 523 | PF00069 | 0.662 |
MOD_ProDKin_1 | 66 | 72 | PF00069 | 0.480 |
MOD_SUMO_for_1 | 430 | 433 | PF00179 | 0.513 |
MOD_SUMO_rev_2 | 392 | 402 | PF00179 | 0.742 |
MOD_SUMO_rev_2 | 545 | 551 | PF00179 | 0.574 |
TRG_DiLeu_BaLyEn_6 | 143 | 148 | PF01217 | 0.214 |
TRG_DiLeu_BaLyEn_6 | 48 | 53 | PF01217 | 0.540 |
TRG_ENDOCYTIC_2 | 119 | 122 | PF00928 | 0.453 |
TRG_ENDOCYTIC_2 | 362 | 365 | PF00928 | 0.580 |
TRG_ER_diArg_1 | 192 | 195 | PF00400 | 0.682 |
TRG_ER_diArg_1 | 514 | 516 | PF00400 | 0.685 |
TRG_NES_CRM1_1 | 282 | 294 | PF08389 | 0.690 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IJN9 | Leptomonas seymouri | 40% | 82% |
A0A3Q8ITN7 | Leishmania donovani | 82% | 100% |
A4HKY8 | Leishmania braziliensis | 58% | 100% |
A4I8G9 | Leishmania infantum | 82% | 100% |
Q4Q4S7 | Leishmania major | 81% | 100% |