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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
Related structures:
AlphaFold database: A4HNC5
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 | 11 |
GO:0140104 | molecular carrier activity | 1 | 11 |
GO:0140597 | protein carrier chaperone | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 542 | 546 | PF00656 | 0.658 |
CLV_NRD_NRD_1 | 184 | 186 | PF00675 | 0.313 |
CLV_NRD_NRD_1 | 320 | 322 | PF00675 | 0.367 |
CLV_PCSK_KEX2_1 | 184 | 186 | PF00082 | 0.310 |
CLV_PCSK_KEX2_1 | 320 | 322 | PF00082 | 0.362 |
CLV_PCSK_KEX2_1 | 512 | 514 | PF00082 | 0.568 |
CLV_PCSK_PC1ET2_1 | 512 | 514 | PF00082 | 0.568 |
CLV_PCSK_SKI1_1 | 146 | 150 | PF00082 | 0.351 |
CLV_PCSK_SKI1_1 | 185 | 189 | PF00082 | 0.295 |
CLV_PCSK_SKI1_1 | 264 | 268 | PF00082 | 0.351 |
CLV_PCSK_SKI1_1 | 350 | 354 | PF00082 | 0.443 |
DEG_APCC_DBOX_1 | 145 | 153 | PF00400 | 0.604 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.509 |
DOC_CDC14_PxL_1 | 243 | 251 | PF14671 | 0.335 |
DOC_CKS1_1 | 28 | 33 | PF01111 | 0.400 |
DOC_CYCLIN_RxL_1 | 315 | 329 | PF00134 | 0.504 |
DOC_CYCLIN_yCln2_LP_2 | 239 | 245 | PF00134 | 0.292 |
DOC_CYCLIN_yCln2_LP_2 | 308 | 314 | PF00134 | 0.306 |
DOC_MAPK_MEF2A_6 | 140 | 149 | PF00069 | 0.587 |
DOC_MAPK_MEF2A_6 | 293 | 300 | PF00069 | 0.236 |
DOC_MAPK_MEF2A_6 | 386 | 393 | PF00069 | 0.549 |
DOC_PP1_RVXF_1 | 159 | 165 | PF00149 | 0.553 |
DOC_PP1_RVXF_1 | 270 | 277 | PF00149 | 0.472 |
DOC_PP1_RVXF_1 | 319 | 326 | PF00149 | 0.590 |
DOC_PP2B_LxvP_1 | 147 | 150 | PF13499 | 0.536 |
DOC_PP2B_LxvP_1 | 237 | 240 | PF13499 | 0.315 |
DOC_PP2B_LxvP_1 | 244 | 247 | PF13499 | 0.314 |
DOC_PP4_FxxP_1 | 325 | 328 | PF00568 | 0.488 |
DOC_USP7_MATH_1 | 287 | 291 | PF00917 | 0.193 |
DOC_USP7_MATH_1 | 336 | 340 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 346 | 350 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 476 | 480 | PF00917 | 0.731 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.413 |
DOC_USP7_MATH_1 | 96 | 100 | PF00917 | 0.442 |
DOC_USP7_UBL2_3 | 413 | 417 | PF12436 | 0.755 |
DOC_USP7_UBL2_3 | 512 | 516 | PF12436 | 0.798 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.556 |
DOC_WW_Pin1_4 | 21 | 26 | PF00397 | 0.449 |
DOC_WW_Pin1_4 | 27 | 32 | PF00397 | 0.416 |
DOC_WW_Pin1_4 | 313 | 318 | PF00397 | 0.285 |
DOC_WW_Pin1_4 | 324 | 329 | PF00397 | 0.650 |
DOC_WW_Pin1_4 | 332 | 337 | PF00397 | 0.680 |
DOC_WW_Pin1_4 | 427 | 432 | PF00397 | 0.681 |
DOC_WW_Pin1_4 | 466 | 471 | PF00397 | 0.754 |
DOC_WW_Pin1_4 | 479 | 484 | PF00397 | 0.697 |
DOC_WW_Pin1_4 | 499 | 504 | PF00397 | 0.728 |
DOC_WW_Pin1_4 | 537 | 542 | PF00397 | 0.767 |
DOC_WW_Pin1_4 | 550 | 555 | PF00397 | 0.738 |
LIG_14-3-3_CanoR_1 | 128 | 133 | PF00244 | 0.271 |
LIG_14-3-3_CanoR_1 | 184 | 188 | PF00244 | 0.519 |
LIG_14-3-3_CanoR_1 | 3 | 11 | PF00244 | 0.410 |
LIG_14-3-3_CanoR_1 | 350 | 355 | PF00244 | 0.644 |
LIG_14-3-3_CanoR_1 | 518 | 523 | PF00244 | 0.634 |
LIG_APCC_ABBA_1 | 134 | 139 | PF00400 | 0.330 |
LIG_BRCT_BRCA1_1 | 74 | 78 | PF00533 | 0.376 |
LIG_Clathr_ClatBox_1 | 255 | 259 | PF01394 | 0.338 |
LIG_deltaCOP1_diTrp_1 | 70 | 78 | PF00928 | 0.336 |
LIG_FHA_1 | 116 | 122 | PF00498 | 0.356 |
LIG_FHA_1 | 13 | 19 | PF00498 | 0.454 |
LIG_FHA_1 | 191 | 197 | PF00498 | 0.568 |
LIG_FHA_1 | 248 | 254 | PF00498 | 0.335 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.451 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.479 |
LIG_FHA_1 | 460 | 466 | PF00498 | 0.669 |
LIG_FHA_2 | 236 | 242 | PF00498 | 0.295 |
LIG_FHA_2 | 351 | 357 | PF00498 | 0.640 |
LIG_FHA_2 | 62 | 68 | PF00498 | 0.377 |
LIG_LIR_Gen_1 | 157 | 167 | PF02991 | 0.517 |
LIG_LIR_Gen_1 | 341 | 352 | PF02991 | 0.560 |
LIG_LIR_Gen_1 | 99 | 106 | PF02991 | 0.293 |
LIG_LIR_Nem_3 | 131 | 137 | PF02991 | 0.290 |
LIG_LIR_Nem_3 | 157 | 162 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 186 | 191 | PF02991 | 0.527 |
LIG_LIR_Nem_3 | 341 | 347 | PF02991 | 0.565 |
LIG_LIR_Nem_3 | 390 | 396 | PF02991 | 0.624 |
LIG_LIR_Nem_3 | 62 | 68 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 75 | 81 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 99 | 104 | PF02991 | 0.268 |
LIG_NRBOX | 251 | 257 | PF00104 | 0.193 |
LIG_NRBOX | 395 | 401 | PF00104 | 0.657 |
LIG_Pex14_2 | 101 | 105 | PF04695 | 0.298 |
LIG_SH2_GRB2like | 163 | 166 | PF00017 | 0.618 |
LIG_SH2_SRC | 299 | 302 | PF00017 | 0.215 |
LIG_SH2_STAT5 | 163 | 166 | PF00017 | 0.569 |
LIG_SH2_STAT5 | 231 | 234 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 299 | 302 | PF00017 | 0.271 |
LIG_SH2_STAT5 | 395 | 398 | PF00017 | 0.605 |
LIG_SH2_STAT5 | 441 | 444 | PF00017 | 0.799 |
LIG_SH2_STAT5 | 65 | 68 | PF00017 | 0.354 |
LIG_SH3_3 | 538 | 544 | PF00018 | 0.774 |
LIG_SH3_3 | 545 | 551 | PF00018 | 0.774 |
LIG_SH3_3 | 8 | 14 | PF00018 | 0.386 |
LIG_SUMO_SIM_anti_2 | 118 | 123 | PF11976 | 0.325 |
LIG_SUMO_SIM_anti_2 | 241 | 248 | PF11976 | 0.181 |
LIG_SUMO_SIM_par_1 | 117 | 123 | PF11976 | 0.299 |
LIG_SUMO_SIM_par_1 | 205 | 210 | PF11976 | 0.193 |
LIG_SUMO_SIM_par_1 | 241 | 248 | PF11976 | 0.201 |
LIG_SUMO_SIM_par_1 | 310 | 316 | PF11976 | 0.289 |
LIG_WRC_WIRS_1 | 289 | 294 | PF05994 | 0.381 |
MOD_CDK_SPxxK_3 | 313 | 320 | PF00069 | 0.274 |
MOD_CDK_SPxxK_3 | 466 | 473 | PF00069 | 0.772 |
MOD_CK1_1 | 20 | 26 | PF00069 | 0.459 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.230 |
MOD_CK1_1 | 291 | 297 | PF00069 | 0.307 |
MOD_CK1_1 | 479 | 485 | PF00069 | 0.708 |
MOD_CK1_1 | 490 | 496 | PF00069 | 0.671 |
MOD_CK1_1 | 549 | 555 | PF00069 | 0.723 |
MOD_CK1_1 | 99 | 105 | PF00069 | 0.395 |
MOD_CK2_1 | 166 | 172 | PF00069 | 0.604 |
MOD_CK2_1 | 350 | 356 | PF00069 | 0.642 |
MOD_CK2_1 | 479 | 485 | PF00069 | 0.728 |
MOD_CK2_1 | 530 | 536 | PF00069 | 0.651 |
MOD_CK2_1 | 61 | 67 | PF00069 | 0.388 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.328 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.537 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.547 |
MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.510 |
MOD_GlcNHglycan | 489 | 492 | PF01048 | 0.566 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.684 |
MOD_GlcNHglycan | 506 | 509 | PF01048 | 0.420 |
MOD_GlcNHglycan | 524 | 527 | PF01048 | 0.578 |
MOD_GlcNHglycan | 528 | 531 | PF01048 | 0.483 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.537 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.561 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.279 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.262 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.475 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.564 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.424 |
MOD_GSK3_1 | 287 | 294 | PF00069 | 0.391 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.649 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.673 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.443 |
MOD_GSK3_1 | 475 | 482 | PF00069 | 0.692 |
MOD_GSK3_1 | 517 | 524 | PF00069 | 0.724 |
MOD_GSK3_1 | 526 | 533 | PF00069 | 0.720 |
MOD_GSK3_1 | 546 | 553 | PF00069 | 0.587 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.420 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.413 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.431 |
MOD_N-GLC_1 | 47 | 52 | PF02516 | 0.684 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.367 |
MOD_NEK2_1 | 132 | 137 | PF00069 | 0.288 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.455 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.318 |
MOD_NEK2_1 | 337 | 342 | PF00069 | 0.566 |
MOD_NEK2_1 | 385 | 390 | PF00069 | 0.688 |
MOD_NEK2_1 | 49 | 54 | PF00069 | 0.453 |
MOD_NEK2_1 | 517 | 522 | PF00069 | 0.715 |
MOD_NEK2_1 | 72 | 77 | PF00069 | 0.378 |
MOD_PIKK_1 | 553 | 559 | PF00454 | 0.686 |
MOD_PIKK_1 | 59 | 65 | PF00454 | 0.331 |
MOD_PIKK_1 | 99 | 105 | PF00454 | 0.430 |
MOD_PKA_2 | 183 | 189 | PF00069 | 0.449 |
MOD_PKA_2 | 459 | 465 | PF00069 | 0.663 |
MOD_PKA_2 | 487 | 493 | PF00069 | 0.706 |
MOD_PKA_2 | 517 | 523 | PF00069 | 0.664 |
MOD_PKB_1 | 348 | 356 | PF00069 | 0.740 |
MOD_Plk_4 | 115 | 121 | PF00069 | 0.331 |
MOD_Plk_4 | 128 | 134 | PF00069 | 0.314 |
MOD_Plk_4 | 175 | 181 | PF00069 | 0.595 |
MOD_Plk_4 | 227 | 233 | PF00069 | 0.336 |
MOD_Plk_4 | 61 | 67 | PF00069 | 0.374 |
MOD_Plk_4 | 96 | 102 | PF00069 | 0.414 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.557 |
MOD_ProDKin_1 | 21 | 27 | PF00069 | 0.446 |
MOD_ProDKin_1 | 313 | 319 | PF00069 | 0.284 |
MOD_ProDKin_1 | 324 | 330 | PF00069 | 0.654 |
MOD_ProDKin_1 | 332 | 338 | PF00069 | 0.686 |
MOD_ProDKin_1 | 427 | 433 | PF00069 | 0.679 |
MOD_ProDKin_1 | 466 | 472 | PF00069 | 0.756 |
MOD_ProDKin_1 | 479 | 485 | PF00069 | 0.697 |
MOD_ProDKin_1 | 499 | 505 | PF00069 | 0.728 |
MOD_ProDKin_1 | 537 | 543 | PF00069 | 0.769 |
MOD_ProDKin_1 | 550 | 556 | PF00069 | 0.737 |
MOD_SUMO_rev_2 | 259 | 268 | PF00179 | 0.550 |
TRG_DiLeu_BaEn_1 | 115 | 120 | PF01217 | 0.300 |
TRG_DiLeu_BaLyEn_6 | 239 | 244 | PF01217 | 0.238 |
TRG_DiLeu_BaLyEn_6 | 308 | 313 | PF01217 | 0.322 |
TRG_ER_diArg_1 | 144 | 147 | PF00400 | 0.526 |
TRG_ER_diArg_1 | 319 | 321 | PF00400 | 0.548 |
TRG_ER_diArg_1 | 347 | 350 | PF00400 | 0.554 |
TRG_ER_diArg_1 | 423 | 426 | PF00400 | 0.714 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PFR8 | Leptomonas seymouri | 54% | 100% |
A0A1X0P4X1 | Trypanosomatidae | 40% | 100% |
A0A3S7XA08 | Leishmania donovani | 76% | 100% |
A0A422P166 | Trypanosoma rangeli | 38% | 100% |
A4IBZ8 | Leishmania infantum | 76% | 100% |
C9ZYK6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
E9AFT5 | Leishmania major | 76% | 100% |
E9B6Y7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 100% |
V5BT14 | Trypanosoma cruzi | 39% | 100% |