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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
Related structures:
AlphaFold database: A4IBZ8
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0006839 | mitochondrial transport | 4 | 1 |
GO:0006886 | intracellular protein transport | 4 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007005 | mitochondrion organization | 5 | 1 |
GO:0007006 | mitochondrial membrane organization | 5 | 1 |
GO:0008104 | protein localization | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0015031 | protein transport | 4 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0032978 | protein insertion into membrane from inner side | 6 | 1 |
GO:0032979 | protein insertion into mitochondrial inner membrane from matrix | 5 | 1 |
GO:0033036 | macromolecule localization | 2 | 1 |
GO:0033365 | protein localization to organelle | 5 | 1 |
GO:0045184 | establishment of protein localization | 3 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051205 | protein insertion into membrane | 5 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0051668 | localization within membrane | 3 | 1 |
GO:0061024 | membrane organization | 4 | 1 |
GO:0070585 | protein localization to mitochondrion | 6 | 1 |
GO:0070727 | cellular macromolecule localization | 3 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
GO:0071705 | nitrogen compound transport | 4 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0072594 | establishment of protein localization to organelle | 4 | 1 |
GO:0072655 | establishment of protein localization to mitochondrion | 5 | 1 |
GO:0072657 | protein localization to membrane | 4 | 1 |
GO:0090150 | establishment of protein localization to membrane | 4 | 1 |
GO:0090151 | establishment of protein localization to mitochondrial membrane | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0032977 | membrane insertase activity | 3 | 10 |
GO:0140104 | molecular carrier activity | 1 | 10 |
GO:0140597 | protein carrier chaperone | 2 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 490 | 494 | PF00656 | 0.684 |
CLV_NRD_NRD_1 | 183 | 185 | PF00675 | 0.309 |
CLV_NRD_NRD_1 | 319 | 321 | PF00675 | 0.355 |
CLV_NRD_NRD_1 | 336 | 338 | PF00675 | 0.495 |
CLV_PCSK_KEX2_1 | 183 | 185 | PF00082 | 0.323 |
CLV_PCSK_KEX2_1 | 319 | 321 | PF00082 | 0.350 |
CLV_PCSK_KEX2_1 | 336 | 338 | PF00082 | 0.495 |
CLV_PCSK_KEX2_1 | 510 | 512 | PF00082 | 0.502 |
CLV_PCSK_PC1ET2_1 | 510 | 512 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 145 | 149 | PF00082 | 0.340 |
CLV_PCSK_SKI1_1 | 184 | 188 | PF00082 | 0.311 |
CLV_PCSK_SKI1_1 | 263 | 267 | PF00082 | 0.356 |
CLV_PCSK_SKI1_1 | 337 | 341 | PF00082 | 0.437 |
CLV_PCSK_SKI1_1 | 349 | 353 | PF00082 | 0.433 |
DEG_APCC_DBOX_1 | 144 | 152 | PF00400 | 0.594 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.431 |
DEG_ODPH_VHL_1 | 54 | 67 | PF01847 | 0.377 |
DEG_SCF_FBW7_1 | 27 | 34 | PF00400 | 0.494 |
DEG_SCF_FBW7_1 | 333 | 338 | PF00400 | 0.558 |
DEG_SPOP_SBC_1 | 225 | 229 | PF00917 | 0.314 |
DEG_SPOP_SBC_1 | 473 | 477 | PF00917 | 0.678 |
DOC_CDC14_PxL_1 | 242 | 250 | PF14671 | 0.341 |
DOC_CDC14_PxL_1 | 282 | 290 | PF14671 | 0.297 |
DOC_CKS1_1 | 465 | 470 | PF01111 | 0.674 |
DOC_CYCLIN_RxL_1 | 314 | 328 | PF00134 | 0.503 |
DOC_CYCLIN_yCln2_LP_2 | 238 | 244 | PF00134 | 0.325 |
DOC_CYCLIN_yCln2_LP_2 | 307 | 313 | PF00134 | 0.312 |
DOC_MAPK_MEF2A_6 | 139 | 148 | PF00069 | 0.576 |
DOC_MAPK_MEF2A_6 | 292 | 299 | PF00069 | 0.259 |
DOC_PP1_RVXF_1 | 158 | 164 | PF00149 | 0.547 |
DOC_PP1_RVXF_1 | 269 | 276 | PF00149 | 0.484 |
DOC_PP1_RVXF_1 | 318 | 325 | PF00149 | 0.574 |
DOC_PP2B_LxvP_1 | 146 | 149 | PF13499 | 0.540 |
DOC_PP2B_LxvP_1 | 236 | 239 | PF13499 | 0.304 |
DOC_PP2B_LxvP_1 | 54 | 57 | PF13499 | 0.429 |
DOC_PP4_FxxP_1 | 11 | 14 | PF00568 | 0.549 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.511 |
DOC_USP7_MATH_1 | 335 | 339 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 429 | 433 | PF00917 | 0.775 |
DOC_USP7_MATH_1 | 451 | 455 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.561 |
DOC_USP7_MATH_1 | 474 | 478 | PF00917 | 0.710 |
DOC_USP7_MATH_1 | 481 | 485 | PF00917 | 0.661 |
DOC_USP7_MATH_1 | 487 | 491 | PF00917 | 0.748 |
DOC_USP7_MATH_1 | 515 | 519 | PF00917 | 0.726 |
DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.425 |
DOC_USP7_UBL2_3 | 412 | 416 | PF12436 | 0.710 |
DOC_USP7_UBL2_3 | 510 | 514 | PF12436 | 0.700 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.515 |
DOC_WW_Pin1_4 | 27 | 32 | PF00397 | 0.455 |
DOC_WW_Pin1_4 | 331 | 336 | PF00397 | 0.671 |
DOC_WW_Pin1_4 | 42 | 47 | PF00397 | 0.362 |
DOC_WW_Pin1_4 | 464 | 469 | PF00397 | 0.725 |
DOC_WW_Pin1_4 | 477 | 482 | PF00397 | 0.745 |
DOC_WW_Pin1_4 | 542 | 547 | PF00397 | 0.734 |
DOC_WW_Pin1_4 | 548 | 553 | PF00397 | 0.702 |
LIG_14-3-3_CanoR_1 | 127 | 132 | PF00244 | 0.276 |
LIG_14-3-3_CanoR_1 | 336 | 342 | PF00244 | 0.645 |
LIG_14-3-3_CanoR_1 | 349 | 354 | PF00244 | 0.636 |
LIG_14-3-3_CanoR_1 | 427 | 435 | PF00244 | 0.692 |
LIG_Actin_WH2_2 | 298 | 316 | PF00022 | 0.312 |
LIG_AP2alpha_2 | 240 | 242 | PF02296 | 0.310 |
LIG_APCC_ABBA_1 | 133 | 138 | PF00400 | 0.335 |
LIG_BIR_III_2 | 493 | 497 | PF00653 | 0.615 |
LIG_BRCT_BRCA1_1 | 73 | 77 | PF00533 | 0.446 |
LIG_Clathr_ClatBox_1 | 254 | 258 | PF01394 | 0.276 |
LIG_deltaCOP1_diTrp_1 | 69 | 77 | PF00928 | 0.329 |
LIG_eIF4E_1 | 5 | 11 | PF01652 | 0.394 |
LIG_FHA_1 | 115 | 121 | PF00498 | 0.365 |
LIG_FHA_1 | 190 | 196 | PF00498 | 0.548 |
LIG_FHA_1 | 247 | 253 | PF00498 | 0.398 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.424 |
LIG_FHA_2 | 235 | 241 | PF00498 | 0.326 |
LIG_FHA_2 | 350 | 356 | PF00498 | 0.630 |
LIG_FHA_2 | 61 | 67 | PF00498 | 0.377 |
LIG_LIR_Gen_1 | 156 | 166 | PF02991 | 0.525 |
LIG_LIR_Gen_1 | 240 | 248 | PF02991 | 0.281 |
LIG_LIR_Gen_1 | 404 | 414 | PF02991 | 0.608 |
LIG_LIR_Gen_1 | 63 | 71 | PF02991 | 0.322 |
LIG_LIR_Gen_1 | 98 | 105 | PF02991 | 0.303 |
LIG_LIR_Nem_3 | 130 | 136 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 156 | 161 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 240 | 245 | PF02991 | 0.244 |
LIG_LIR_Nem_3 | 389 | 395 | PF02991 | 0.664 |
LIG_LIR_Nem_3 | 404 | 409 | PF02991 | 0.684 |
LIG_LIR_Nem_3 | 63 | 67 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 74 | 80 | PF02991 | 0.395 |
LIG_NRBOX | 394 | 400 | PF00104 | 0.639 |
LIG_Pex14_2 | 100 | 104 | PF04695 | 0.294 |
LIG_SH2_CRK | 5 | 9 | PF00017 | 0.391 |
LIG_SH2_GRB2like | 162 | 165 | PF00017 | 0.555 |
LIG_SH2_STAT5 | 162 | 165 | PF00017 | 0.559 |
LIG_SH2_STAT5 | 230 | 233 | PF00017 | 0.331 |
LIG_SH2_STAT5 | 298 | 301 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 394 | 397 | PF00017 | 0.588 |
LIG_SH2_STAT5 | 64 | 67 | PF00017 | 0.362 |
LIG_SH3_3 | 50 | 56 | PF00018 | 0.493 |
LIG_SH3_3 | 509 | 515 | PF00018 | 0.668 |
LIG_SH3_3 | 543 | 549 | PF00018 | 0.738 |
LIG_SUMO_SIM_anti_2 | 117 | 122 | PF11976 | 0.363 |
LIG_SUMO_SIM_par_1 | 309 | 315 | PF11976 | 0.276 |
LIG_TRAF2_1 | 326 | 329 | PF00917 | 0.502 |
LIG_WRC_WIRS_1 | 288 | 293 | PF05994 | 0.383 |
MOD_CDK_SPK_2 | 10 | 15 | PF00069 | 0.378 |
MOD_CDK_SPK_2 | 331 | 336 | PF00069 | 0.593 |
MOD_CDK_SPxK_1 | 331 | 337 | PF00069 | 0.609 |
MOD_CDK_SPxxK_3 | 10 | 17 | PF00069 | 0.363 |
MOD_CDK_SPxxK_3 | 464 | 471 | PF00069 | 0.729 |
MOD_CK1_1 | 290 | 296 | PF00069 | 0.391 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.433 |
MOD_CK1_1 | 477 | 483 | PF00069 | 0.676 |
MOD_CK1_1 | 502 | 508 | PF00069 | 0.688 |
MOD_CK1_1 | 542 | 548 | PF00069 | 0.745 |
MOD_CK1_1 | 550 | 556 | PF00069 | 0.718 |
MOD_CK1_1 | 98 | 104 | PF00069 | 0.366 |
MOD_CK2_1 | 165 | 171 | PF00069 | 0.545 |
MOD_CK2_1 | 323 | 329 | PF00069 | 0.551 |
MOD_CK2_1 | 349 | 355 | PF00069 | 0.634 |
MOD_CK2_1 | 477 | 483 | PF00069 | 0.794 |
MOD_CK2_1 | 528 | 534 | PF00069 | 0.608 |
MOD_GlcNHglycan | 167 | 170 | PF01048 | 0.313 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.526 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.499 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.327 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.288 |
MOD_GlcNHglycan | 337 | 340 | PF01048 | 0.527 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.503 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.694 |
MOD_GlcNHglycan | 421 | 425 | PF01048 | 0.556 |
MOD_GlcNHglycan | 445 | 448 | PF01048 | 0.435 |
MOD_GlcNHglycan | 483 | 486 | PF01048 | 0.512 |
MOD_GlcNHglycan | 489 | 493 | PF01048 | 0.522 |
MOD_GlcNHglycan | 501 | 504 | PF01048 | 0.409 |
MOD_GlcNHglycan | 522 | 525 | PF01048 | 0.501 |
MOD_GlcNHglycan | 542 | 545 | PF01048 | 0.502 |
MOD_GlcNHglycan | 81 | 85 | PF01048 | 0.631 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.667 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.277 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.563 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.335 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.464 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.513 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.634 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.404 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.627 |
MOD_GSK3_1 | 473 | 480 | PF00069 | 0.675 |
MOD_GSK3_1 | 498 | 505 | PF00069 | 0.702 |
MOD_GSK3_1 | 515 | 522 | PF00069 | 0.706 |
MOD_GSK3_1 | 524 | 531 | PF00069 | 0.655 |
MOD_GSK3_1 | 540 | 547 | PF00069 | 0.722 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.399 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.414 |
MOD_N-GLC_1 | 219 | 224 | PF02516 | 0.530 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.364 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.294 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.337 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.480 |
MOD_NEK2_1 | 312 | 317 | PF00069 | 0.392 |
MOD_NEK2_1 | 384 | 389 | PF00069 | 0.628 |
MOD_NEK2_1 | 443 | 448 | PF00069 | 0.653 |
MOD_NEK2_1 | 520 | 525 | PF00069 | 0.689 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.365 |
MOD_NEK2_2 | 31 | 36 | PF00069 | 0.412 |
MOD_NEK2_2 | 370 | 375 | PF00069 | 0.606 |
MOD_NEK2_2 | 515 | 520 | PF00069 | 0.619 |
MOD_PIKK_1 | 525 | 531 | PF00454 | 0.650 |
MOD_PIKK_1 | 551 | 557 | PF00454 | 0.661 |
MOD_PIKK_1 | 98 | 104 | PF00454 | 0.348 |
MOD_PKA_2 | 335 | 341 | PF00069 | 0.641 |
MOD_PKB_1 | 425 | 433 | PF00069 | 0.613 |
MOD_Plk_1 | 219 | 225 | PF00069 | 0.399 |
MOD_Plk_1 | 257 | 263 | PF00069 | 0.488 |
MOD_Plk_2-3 | 219 | 225 | PF00069 | 0.323 |
MOD_Plk_4 | 114 | 120 | PF00069 | 0.306 |
MOD_Plk_4 | 127 | 133 | PF00069 | 0.210 |
MOD_Plk_4 | 174 | 180 | PF00069 | 0.534 |
MOD_Plk_4 | 226 | 232 | PF00069 | 0.294 |
MOD_Plk_4 | 515 | 521 | PF00069 | 0.619 |
MOD_Plk_4 | 60 | 66 | PF00069 | 0.404 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.410 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.515 |
MOD_ProDKin_1 | 27 | 33 | PF00069 | 0.456 |
MOD_ProDKin_1 | 331 | 337 | PF00069 | 0.679 |
MOD_ProDKin_1 | 42 | 48 | PF00069 | 0.356 |
MOD_ProDKin_1 | 464 | 470 | PF00069 | 0.739 |
MOD_ProDKin_1 | 477 | 483 | PF00069 | 0.744 |
MOD_ProDKin_1 | 542 | 548 | PF00069 | 0.737 |
MOD_SUMO_rev_2 | 258 | 267 | PF00179 | 0.604 |
TRG_DiLeu_BaEn_1 | 114 | 119 | PF01217 | 0.276 |
TRG_DiLeu_BaLyEn_6 | 307 | 312 | PF01217 | 0.308 |
TRG_ENDOCYTIC_2 | 406 | 409 | PF00928 | 0.604 |
TRG_ENDOCYTIC_2 | 64 | 67 | PF00928 | 0.345 |
TRG_ER_diArg_1 | 143 | 146 | PF00400 | 0.533 |
TRG_ER_diArg_1 | 318 | 320 | PF00400 | 0.537 |
TRG_ER_diArg_1 | 335 | 337 | PF00400 | 0.691 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PFR8 | Leptomonas seymouri | 55% | 100% |
A0A0S4JMC8 | Bodo saltans | 35% | 100% |
A0A3S7XA08 | Leishmania donovani | 100% | 100% |
A0A422P166 | Trypanosoma rangeli | 39% | 100% |
A4HNC5 | Leishmania braziliensis | 76% | 100% |
E9AFT5 | Leishmania major | 91% | 100% |
E9B6Y7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
V5BT14 | Trypanosoma cruzi | 39% | 100% |