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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: Q4Q7K1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 308 | 312 | PF00656 | 0.669 |
CLV_C14_Caspase3-7 | 49 | 53 | PF00656 | 0.721 |
CLV_NRD_NRD_1 | 138 | 140 | PF00675 | 0.591 |
CLV_NRD_NRD_1 | 246 | 248 | PF00675 | 0.670 |
CLV_NRD_NRD_1 | 35 | 37 | PF00675 | 0.783 |
CLV_NRD_NRD_1 | 389 | 391 | PF00675 | 0.609 |
CLV_NRD_NRD_1 | 438 | 440 | PF00675 | 0.549 |
CLV_NRD_NRD_1 | 54 | 56 | PF00675 | 0.578 |
CLV_PCSK_FUR_1 | 21 | 25 | PF00082 | 0.684 |
CLV_PCSK_FUR_1 | 244 | 248 | PF00082 | 0.697 |
CLV_PCSK_FUR_1 | 39 | 43 | PF00082 | 0.533 |
CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.591 |
CLV_PCSK_KEX2_1 | 23 | 25 | PF00082 | 0.690 |
CLV_PCSK_KEX2_1 | 246 | 248 | PF00082 | 0.638 |
CLV_PCSK_KEX2_1 | 365 | 367 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 41 | 43 | PF00082 | 0.535 |
CLV_PCSK_KEX2_1 | 438 | 440 | PF00082 | 0.515 |
CLV_PCSK_KEX2_1 | 54 | 56 | PF00082 | 0.621 |
CLV_PCSK_PC1ET2_1 | 23 | 25 | PF00082 | 0.690 |
CLV_PCSK_PC1ET2_1 | 365 | 367 | PF00082 | 0.541 |
CLV_PCSK_PC1ET2_1 | 41 | 43 | PF00082 | 0.535 |
CLV_PCSK_PC7_1 | 19 | 25 | PF00082 | 0.679 |
CLV_PCSK_SKI1_1 | 15 | 19 | PF00082 | 0.619 |
CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.534 |
CLV_PCSK_SKI1_1 | 173 | 177 | PF00082 | 0.576 |
CLV_PCSK_SKI1_1 | 193 | 197 | PF00082 | 0.322 |
CLV_PCSK_SKI1_1 | 390 | 394 | PF00082 | 0.607 |
CLV_Separin_Metazoa | 340 | 344 | PF03568 | 0.546 |
CLV_Separin_Metazoa | 415 | 419 | PF03568 | 0.599 |
DEG_APCC_DBOX_1 | 172 | 180 | PF00400 | 0.534 |
DEG_APCC_DBOX_1 | 231 | 239 | PF00400 | 0.476 |
DEG_APCC_DBOX_1 | 409 | 417 | PF00400 | 0.502 |
DEG_APCC_DBOX_1 | 437 | 445 | PF00400 | 0.547 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.617 |
DEG_SPOP_SBC_1 | 275 | 279 | PF00917 | 0.586 |
DOC_CYCLIN_RxL_1 | 473 | 484 | PF00134 | 0.555 |
DOC_CYCLIN_yCln2_LP_2 | 321 | 327 | PF00134 | 0.682 |
DOC_MAPK_DCC_7 | 438 | 446 | PF00069 | 0.526 |
DOC_MAPK_gen_1 | 365 | 371 | PF00069 | 0.548 |
DOC_MAPK_gen_1 | 390 | 399 | PF00069 | 0.730 |
DOC_MAPK_gen_1 | 438 | 446 | PF00069 | 0.478 |
DOC_MAPK_MEF2A_6 | 244 | 252 | PF00069 | 0.606 |
DOC_MAPK_MEF2A_6 | 438 | 447 | PF00069 | 0.473 |
DOC_PP2B_LxvP_1 | 76 | 79 | PF13499 | 0.568 |
DOC_USP7_MATH_1 | 293 | 297 | PF00917 | 0.744 |
DOC_USP7_MATH_1 | 330 | 334 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 359 | 363 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 409 | 413 | PF00917 | 0.526 |
DOC_USP7_MATH_1 | 464 | 468 | PF00917 | 0.719 |
DOC_USP7_MATH_1 | 491 | 495 | PF00917 | 0.574 |
DOC_USP7_UBL2_3 | 37 | 41 | PF12436 | 0.544 |
DOC_WW_Pin1_4 | 199 | 204 | PF00397 | 0.705 |
DOC_WW_Pin1_4 | 239 | 244 | PF00397 | 0.702 |
DOC_WW_Pin1_4 | 257 | 262 | PF00397 | 0.777 |
DOC_WW_Pin1_4 | 263 | 268 | PF00397 | 0.524 |
LIG_14-3-3_CanoR_1 | 193 | 203 | PF00244 | 0.669 |
LIG_14-3-3_CanoR_1 | 223 | 231 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 257 | 261 | PF00244 | 0.688 |
LIG_14-3-3_CanoR_1 | 3 | 9 | PF00244 | 0.648 |
LIG_14-3-3_CanoR_1 | 407 | 417 | PF00244 | 0.531 |
LIG_14-3-3_CanoR_1 | 42 | 50 | PF00244 | 0.636 |
LIG_14-3-3_CanoR_1 | 438 | 442 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 460 | 469 | PF00244 | 0.665 |
LIG_14-3-3_CanoR_1 | 476 | 481 | PF00244 | 0.509 |
LIG_Actin_WH2_2 | 112 | 130 | PF00022 | 0.627 |
LIG_BIR_III_2 | 432 | 436 | PF00653 | 0.685 |
LIG_BIR_III_4 | 328 | 332 | PF00653 | 0.677 |
LIG_BRCT_BRCA1_1 | 13 | 17 | PF00533 | 0.649 |
LIG_BRCT_BRCA1_1 | 259 | 263 | PF00533 | 0.688 |
LIG_BRCT_BRCA1_1 | 276 | 280 | PF00533 | 0.710 |
LIG_BRCT_BRCA1_1 | 483 | 487 | PF00533 | 0.506 |
LIG_Clathr_ClatBox_1 | 444 | 448 | PF01394 | 0.476 |
LIG_CSL_BTD_1 | 504 | 507 | PF09270 | 0.504 |
LIG_deltaCOP1_diTrp_1 | 503 | 511 | PF00928 | 0.546 |
LIG_eIF4E_1 | 225 | 231 | PF01652 | 0.579 |
LIG_EVH1_2 | 267 | 271 | PF00568 | 0.775 |
LIG_FHA_1 | 122 | 128 | PF00498 | 0.595 |
LIG_FHA_1 | 225 | 231 | PF00498 | 0.544 |
LIG_FHA_1 | 279 | 285 | PF00498 | 0.707 |
LIG_FHA_1 | 376 | 382 | PF00498 | 0.773 |
LIG_FHA_1 | 387 | 393 | PF00498 | 0.673 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.771 |
LIG_FHA_2 | 3 | 9 | PF00498 | 0.733 |
LIG_FHA_2 | 306 | 312 | PF00498 | 0.742 |
LIG_GBD_Chelix_1 | 157 | 165 | PF00786 | 0.567 |
LIG_IBAR_NPY_1 | 104 | 106 | PF08397 | 0.557 |
LIG_LIR_Apic_2 | 95 | 100 | PF02991 | 0.600 |
LIG_LIR_Gen_1 | 152 | 161 | PF02991 | 0.521 |
LIG_LIR_Gen_1 | 448 | 456 | PF02991 | 0.594 |
LIG_LIR_LC3C_4 | 126 | 131 | PF02991 | 0.352 |
LIG_LIR_Nem_3 | 152 | 157 | PF02991 | 0.549 |
LIG_LIR_Nem_3 | 448 | 452 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 484 | 490 | PF02991 | 0.471 |
LIG_SH2_CRK | 40 | 44 | PF00017 | 0.639 |
LIG_SH2_CRK | 449 | 453 | PF00017 | 0.567 |
LIG_SH2_NCK_1 | 449 | 453 | PF00017 | 0.602 |
LIG_SH2_STAP1 | 449 | 453 | PF00017 | 0.543 |
LIG_SH2_STAT5 | 421 | 424 | PF00017 | 0.479 |
LIG_SH2_STAT5 | 514 | 517 | PF00017 | 0.647 |
LIG_SH3_3 | 128 | 134 | PF00018 | 0.436 |
LIG_SH3_3 | 378 | 384 | PF00018 | 0.676 |
LIG_SUMO_SIM_par_1 | 201 | 207 | PF11976 | 0.563 |
LIG_SUMO_SIM_par_1 | 442 | 448 | PF11976 | 0.483 |
LIG_TRAF2_1 | 88 | 91 | PF00917 | 0.543 |
LIG_TYR_ITIM | 447 | 452 | PF00017 | 0.563 |
MOD_CDK_SPK_2 | 239 | 244 | PF00069 | 0.533 |
MOD_CDK_SPxxK_3 | 239 | 246 | PF00069 | 0.535 |
MOD_CK1_1 | 259 | 265 | PF00069 | 0.717 |
MOD_CK1_1 | 274 | 280 | PF00069 | 0.662 |
MOD_CK1_1 | 364 | 370 | PF00069 | 0.664 |
MOD_CK1_1 | 376 | 382 | PF00069 | 0.649 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.775 |
MOD_CK1_1 | 463 | 469 | PF00069 | 0.685 |
MOD_CK1_1 | 85 | 91 | PF00069 | 0.570 |
MOD_CK2_1 | 300 | 306 | PF00069 | 0.684 |
MOD_CK2_1 | 343 | 349 | PF00069 | 0.531 |
MOD_CK2_1 | 409 | 415 | PF00069 | 0.535 |
MOD_CK2_1 | 85 | 91 | PF00069 | 0.570 |
MOD_Cter_Amidation | 34 | 37 | PF01082 | 0.769 |
MOD_Cter_Amidation | 52 | 55 | PF01082 | 0.581 |
MOD_DYRK1A_RPxSP_1 | 257 | 261 | PF00069 | 0.692 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.584 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.776 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.762 |
MOD_GlcNHglycan | 321 | 324 | PF01048 | 0.701 |
MOD_GlcNHglycan | 344 | 348 | PF01048 | 0.605 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.644 |
MOD_GlcNHglycan | 462 | 465 | PF01048 | 0.687 |
MOD_GlcNHglycan | 483 | 486 | PF01048 | 0.603 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.463 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.559 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.678 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.653 |
MOD_GSK3_1 | 289 | 296 | PF00069 | 0.528 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.645 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.717 |
MOD_GSK3_1 | 460 | 467 | PF00069 | 0.667 |
MOD_LATS_1 | 458 | 464 | PF00433 | 0.548 |
MOD_N-GLC_1 | 100 | 105 | PF02516 | 0.563 |
MOD_N-GLC_1 | 121 | 126 | PF02516 | 0.545 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.545 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.520 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.456 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.676 |
MOD_NEK2_1 | 224 | 229 | PF00069 | 0.559 |
MOD_NEK2_1 | 230 | 235 | PF00069 | 0.632 |
MOD_NEK2_1 | 256 | 261 | PF00069 | 0.599 |
MOD_NEK2_1 | 280 | 285 | PF00069 | 0.688 |
MOD_NEK2_1 | 408 | 413 | PF00069 | 0.582 |
MOD_NEK2_1 | 490 | 495 | PF00069 | 0.565 |
MOD_NEK2_2 | 123 | 128 | PF00069 | 0.379 |
MOD_PIKK_1 | 293 | 299 | PF00454 | 0.756 |
MOD_PIKK_1 | 458 | 464 | PF00454 | 0.719 |
MOD_PK_1 | 42 | 48 | PF00069 | 0.769 |
MOD_PKA_1 | 41 | 47 | PF00069 | 0.637 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.670 |
MOD_PKA_2 | 256 | 262 | PF00069 | 0.687 |
MOD_PKA_2 | 286 | 292 | PF00069 | 0.704 |
MOD_PKA_2 | 30 | 36 | PF00069 | 0.639 |
MOD_PKA_2 | 409 | 415 | PF00069 | 0.519 |
MOD_PKA_2 | 41 | 47 | PF00069 | 0.637 |
MOD_PKA_2 | 437 | 443 | PF00069 | 0.543 |
MOD_Plk_1 | 121 | 127 | PF00069 | 0.536 |
MOD_Plk_1 | 186 | 192 | PF00069 | 0.566 |
MOD_Plk_1 | 447 | 453 | PF00069 | 0.581 |
MOD_Plk_1 | 491 | 497 | PF00069 | 0.518 |
MOD_Plk_2-3 | 207 | 213 | PF00069 | 0.499 |
MOD_Plk_4 | 115 | 121 | PF00069 | 0.524 |
MOD_Plk_4 | 153 | 159 | PF00069 | 0.510 |
MOD_Plk_4 | 280 | 286 | PF00069 | 0.669 |
MOD_Plk_4 | 295 | 301 | PF00069 | 0.564 |
MOD_Plk_4 | 469 | 475 | PF00069 | 0.598 |
MOD_Plk_4 | 491 | 497 | PF00069 | 0.518 |
MOD_ProDKin_1 | 199 | 205 | PF00069 | 0.707 |
MOD_ProDKin_1 | 239 | 245 | PF00069 | 0.703 |
MOD_ProDKin_1 | 257 | 263 | PF00069 | 0.778 |
MOD_SUMO_rev_2 | 111 | 119 | PF00179 | 0.600 |
MOD_SUMO_rev_2 | 155 | 164 | PF00179 | 0.527 |
MOD_SUMO_rev_2 | 201 | 211 | PF00179 | 0.641 |
MOD_SUMO_rev_2 | 328 | 338 | PF00179 | 0.536 |
TRG_DiLeu_BaLyEn_6 | 348 | 353 | PF01217 | 0.522 |
TRG_ENDOCYTIC_2 | 40 | 43 | PF00928 | 0.642 |
TRG_ENDOCYTIC_2 | 449 | 452 | PF00928 | 0.505 |
TRG_ER_diArg_1 | 138 | 140 | PF00400 | 0.580 |
TRG_ER_diArg_1 | 18 | 21 | PF00400 | 0.636 |
TRG_ER_diArg_1 | 231 | 234 | PF00400 | 0.643 |
TRG_ER_diArg_1 | 243 | 246 | PF00400 | 0.671 |
TRG_NLS_Bipartite_1 | 23 | 40 | PF00514 | 0.551 |
TRG_Pf-PMV_PEXEL_1 | 138 | 142 | PF00026 | 0.439 |
TRG_Pf-PMV_PEXEL_1 | 391 | 395 | PF00026 | 0.584 |
TRG_Pf-PMV_PEXEL_1 | 476 | 481 | PF00026 | 0.510 |
TRG_Pf-PMV_PEXEL_1 | 488 | 492 | PF00026 | 0.522 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PGI0 | Leptomonas seymouri | 48% | 93% |
A0A1X0P334 | Trypanosomatidae | 37% | 100% |
A0A3Q8IFQ7 | Leishmania donovani | 91% | 100% |
A4HI57 | Leishmania braziliensis | 75% | 100% |
A4I5D3 | Leishmania infantum | 91% | 100% |
C9ZQR5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
E9B0N1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |