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 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
Related structures:
AlphaFold database: E9AFT5
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 2 |
GO:0006839 | mitochondrial transport | 4 | 2 |
GO:0006886 | intracellular protein transport | 4 | 2 |
GO:0006996 | organelle organization | 4 | 2 |
GO:0007005 | mitochondrion organization | 5 | 2 |
GO:0007006 | mitochondrial membrane organization | 5 | 2 |
GO:0008104 | protein localization | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0015031 | protein transport | 4 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0032978 | protein insertion into membrane from inner side | 6 | 2 |
GO:0032979 | protein insertion into mitochondrial inner membrane from matrix | 5 | 2 |
GO:0033036 | macromolecule localization | 2 | 2 |
GO:0033365 | protein localization to organelle | 5 | 2 |
GO:0045184 | establishment of protein localization | 3 | 2 |
GO:0046907 | intracellular transport | 3 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051205 | protein insertion into membrane | 5 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0051641 | cellular localization | 2 | 2 |
GO:0051649 | establishment of localization in cell | 3 | 2 |
GO:0051668 | localization within membrane | 3 | 2 |
GO:0061024 | membrane organization | 4 | 2 |
GO:0070585 | protein localization to mitochondrion | 6 | 2 |
GO:0070727 | cellular macromolecule localization | 3 | 2 |
GO:0071702 | organic substance transport | 4 | 2 |
GO:0071705 | nitrogen compound transport | 4 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:0072594 | establishment of protein localization to organelle | 4 | 2 |
GO:0072655 | establishment of protein localization to mitochondrion | 5 | 2 |
GO:0072657 | protein localization to membrane | 4 | 2 |
GO:0090150 | establishment of protein localization to membrane | 4 | 2 |
GO:0090151 | establishment of protein localization to mitochondrial membrane | 4 | 2 |
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_NRD_NRD_1 | 157 | 159 | PF00675 | 0.309 |
CLV_NRD_NRD_1 | 293 | 295 | PF00675 | 0.362 |
CLV_NRD_NRD_1 | 310 | 312 | PF00675 | 0.522 |
CLV_PCSK_KEX2_1 | 157 | 159 | PF00082 | 0.307 |
CLV_PCSK_KEX2_1 | 293 | 295 | PF00082 | 0.362 |
CLV_PCSK_KEX2_1 | 310 | 312 | PF00082 | 0.504 |
CLV_PCSK_KEX2_1 | 484 | 486 | PF00082 | 0.567 |
CLV_PCSK_PC1ET2_1 | 484 | 486 | PF00082 | 0.567 |
CLV_PCSK_SKI1_1 | 119 | 123 | PF00082 | 0.357 |
CLV_PCSK_SKI1_1 | 158 | 162 | PF00082 | 0.295 |
CLV_PCSK_SKI1_1 | 237 | 241 | PF00082 | 0.350 |
CLV_PCSK_SKI1_1 | 311 | 315 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 323 | 327 | PF00082 | 0.450 |
DEG_APCC_DBOX_1 | 118 | 126 | PF00400 | 0.610 |
DEG_ODPH_VHL_1 | 28 | 41 | PF01847 | 0.385 |
DEG_SCF_FBW7_1 | 1 | 8 | PF00400 | 0.453 |
DEG_SPOP_SBC_1 | 199 | 203 | PF00917 | 0.367 |
DEG_SPOP_SBC_1 | 447 | 451 | PF00917 | 0.695 |
DOC_CDC14_PxL_1 | 216 | 224 | PF14671 | 0.335 |
DOC_CDC14_PxL_1 | 256 | 264 | PF14671 | 0.292 |
DOC_CKS1_1 | 439 | 444 | PF01111 | 0.683 |
DOC_CYCLIN_yCln2_LP_2 | 212 | 218 | PF00134 | 0.292 |
DOC_CYCLIN_yCln2_LP_2 | 281 | 287 | PF00134 | 0.271 |
DOC_MAPK_FxFP_2 | 296 | 299 | PF00069 | 0.446 |
DOC_MAPK_gen_1 | 328 | 337 | PF00069 | 0.546 |
DOC_MAPK_MEF2A_6 | 113 | 122 | PF00069 | 0.593 |
DOC_MAPK_MEF2A_6 | 266 | 273 | PF00069 | 0.236 |
DOC_PP1_RVXF_1 | 132 | 138 | PF00149 | 0.555 |
DOC_PP1_RVXF_1 | 243 | 250 | PF00149 | 0.472 |
DOC_PP2B_LxvP_1 | 120 | 123 | PF13499 | 0.542 |
DOC_PP2B_LxvP_1 | 210 | 213 | PF13499 | 0.314 |
DOC_PP2B_LxvP_1 | 217 | 220 | PF13499 | 0.314 |
DOC_PP2B_LxvP_1 | 28 | 31 | PF13499 | 0.435 |
DOC_PP4_FxxP_1 | 296 | 299 | PF00568 | 0.463 |
DOC_USP7_MATH_1 | 16 | 20 | PF00917 | 0.528 |
DOC_USP7_MATH_1 | 309 | 313 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 403 | 407 | PF00917 | 0.743 |
DOC_USP7_MATH_1 | 425 | 429 | PF00917 | 0.686 |
DOC_USP7_MATH_1 | 448 | 452 | PF00917 | 0.727 |
DOC_USP7_MATH_1 | 467 | 471 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 489 | 493 | PF00917 | 0.751 |
DOC_USP7_MATH_1 | 69 | 73 | PF00917 | 0.444 |
DOC_USP7_UBL2_3 | 386 | 390 | PF12436 | 0.726 |
DOC_USP7_UBL2_3 | 484 | 488 | PF12436 | 0.799 |
DOC_WW_Pin1_4 | 1 | 6 | PF00397 | 0.398 |
DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.679 |
DOC_WW_Pin1_4 | 438 | 443 | PF00397 | 0.741 |
DOC_WW_Pin1_4 | 451 | 456 | PF00397 | 0.694 |
DOC_WW_Pin1_4 | 516 | 521 | PF00397 | 0.763 |
DOC_WW_Pin1_4 | 522 | 527 | PF00397 | 0.736 |
LIG_14-3-3_CanoR_1 | 10 | 16 | PF00244 | 0.432 |
LIG_14-3-3_CanoR_1 | 101 | 106 | PF00244 | 0.271 |
LIG_14-3-3_CanoR_1 | 310 | 316 | PF00244 | 0.650 |
LIG_14-3-3_CanoR_1 | 323 | 328 | PF00244 | 0.649 |
LIG_14-3-3_CanoR_1 | 359 | 369 | PF00244 | 0.582 |
LIG_14-3-3_CanoR_1 | 432 | 438 | PF00244 | 0.785 |
LIG_Actin_WH2_2 | 272 | 290 | PF00022 | 0.291 |
LIG_AP2alpha_2 | 214 | 216 | PF02296 | 0.317 |
LIG_APCC_ABBA_1 | 107 | 112 | PF00400 | 0.333 |
LIG_BRCT_BRCA1_1 | 47 | 51 | PF00533 | 0.373 |
LIG_Clathr_ClatBox_1 | 228 | 232 | PF01394 | 0.289 |
LIG_deltaCOP1_diTrp_1 | 43 | 51 | PF00928 | 0.334 |
LIG_FHA_1 | 164 | 170 | PF00498 | 0.557 |
LIG_FHA_1 | 2 | 8 | PF00498 | 0.435 |
LIG_FHA_1 | 221 | 227 | PF00498 | 0.389 |
LIG_FHA_2 | 188 | 194 | PF00498 | 0.222 |
LIG_FHA_2 | 209 | 215 | PF00498 | 0.293 |
LIG_FHA_2 | 324 | 330 | PF00498 | 0.641 |
LIG_FHA_2 | 51 | 57 | PF00498 | 0.445 |
LIG_IRF3_LxIS_1 | 73 | 80 | PF10401 | 0.233 |
LIG_LIR_Gen_1 | 130 | 140 | PF02991 | 0.514 |
LIG_LIR_Gen_1 | 214 | 222 | PF02991 | 0.269 |
LIG_LIR_Gen_1 | 378 | 388 | PF02991 | 0.717 |
LIG_LIR_Gen_1 | 72 | 79 | PF02991 | 0.297 |
LIG_LIR_Nem_3 | 104 | 110 | PF02991 | 0.271 |
LIG_LIR_Nem_3 | 130 | 135 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 214 | 219 | PF02991 | 0.223 |
LIG_LIR_Nem_3 | 363 | 369 | PF02991 | 0.621 |
LIG_LIR_Nem_3 | 378 | 383 | PF02991 | 0.640 |
LIG_LIR_Nem_3 | 48 | 54 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 72 | 77 | PF02991 | 0.271 |
LIG_NRBOX | 368 | 374 | PF00104 | 0.648 |
LIG_Pex14_2 | 74 | 78 | PF04695 | 0.302 |
LIG_SH2_GRB2like | 136 | 139 | PF00017 | 0.615 |
LIG_SH2_GRB2like | 515 | 518 | PF00017 | 0.609 |
LIG_SH2_STAT5 | 136 | 139 | PF00017 | 0.566 |
LIG_SH2_STAT5 | 204 | 207 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 272 | 275 | PF00017 | 0.271 |
LIG_SH2_STAT5 | 368 | 371 | PF00017 | 0.595 |
LIG_SH2_STAT5 | 38 | 41 | PF00017 | 0.352 |
LIG_SH3_3 | 24 | 30 | PF00018 | 0.508 |
LIG_SH3_3 | 483 | 489 | PF00018 | 0.683 |
LIG_SH3_3 | 517 | 523 | PF00018 | 0.768 |
LIG_SUMO_SIM_par_1 | 283 | 289 | PF11976 | 0.289 |
LIG_WRC_WIRS_1 | 262 | 267 | PF05994 | 0.379 |
MOD_CDK_SPK_2 | 305 | 310 | PF00069 | 0.591 |
MOD_CDK_SPxK_1 | 305 | 311 | PF00069 | 0.606 |
MOD_CDK_SPxxK_3 | 438 | 445 | PF00069 | 0.761 |
MOD_CDK_SPxxK_3 | 522 | 529 | PF00069 | 0.630 |
MOD_CK1_1 | 264 | 270 | PF00069 | 0.305 |
MOD_CK1_1 | 451 | 457 | PF00069 | 0.704 |
MOD_CK1_1 | 516 | 522 | PF00069 | 0.738 |
MOD_CK1_1 | 524 | 530 | PF00069 | 0.713 |
MOD_CK1_1 | 72 | 78 | PF00069 | 0.399 |
MOD_CK2_1 | 139 | 145 | PF00069 | 0.595 |
MOD_CK2_1 | 187 | 193 | PF00069 | 0.290 |
MOD_CK2_1 | 323 | 329 | PF00069 | 0.646 |
MOD_CK2_1 | 451 | 457 | PF00069 | 0.724 |
MOD_CK2_1 | 467 | 473 | PF00069 | 0.609 |
MOD_CK2_1 | 50 | 56 | PF00069 | 0.398 |
MOD_CK2_1 | 502 | 508 | PF00069 | 0.640 |
MOD_GlcNHglycan | 141 | 144 | PF01048 | 0.317 |
MOD_GlcNHglycan | 18 | 21 | PF01048 | 0.696 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.509 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.324 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.282 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.541 |
MOD_GlcNHglycan | 320 | 323 | PF01048 | 0.524 |
MOD_GlcNHglycan | 419 | 422 | PF01048 | 0.523 |
MOD_GlcNHglycan | 463 | 467 | PF01048 | 0.568 |
MOD_GlcNHglycan | 469 | 472 | PF01048 | 0.512 |
MOD_GlcNHglycan | 473 | 477 | PF01048 | 0.462 |
MOD_GlcNHglycan | 491 | 494 | PF01048 | 0.473 |
MOD_GlcNHglycan | 496 | 499 | PF01048 | 0.578 |
MOD_GlcNHglycan | 55 | 59 | PF01048 | 0.588 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.558 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.445 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.565 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.425 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.397 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.390 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.649 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.626 |
MOD_GSK3_1 | 447 | 454 | PF00069 | 0.686 |
MOD_GSK3_1 | 467 | 474 | PF00069 | 0.582 |
MOD_GSK3_1 | 489 | 496 | PF00069 | 0.728 |
MOD_GSK3_1 | 498 | 505 | PF00069 | 0.714 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.407 |
MOD_GSK3_1 | 518 | 525 | PF00069 | 0.583 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.427 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.278 |
MOD_N-GLC_1 | 193 | 198 | PF02516 | 0.532 |
MOD_N-GLC_1 | 348 | 353 | PF02516 | 0.366 |
MOD_N-GLC_1 | 516 | 521 | PF02516 | 0.414 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.259 |
MOD_NEK2_1 | 205 | 210 | PF00069 | 0.320 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.481 |
MOD_NEK2_1 | 286 | 291 | PF00069 | 0.385 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.680 |
MOD_NEK2_1 | 417 | 422 | PF00069 | 0.661 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.374 |
MOD_NEK2_1 | 494 | 499 | PF00069 | 0.701 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.334 |
MOD_NEK2_2 | 5 | 10 | PF00069 | 0.408 |
MOD_PIKK_1 | 499 | 505 | PF00454 | 0.645 |
MOD_PIKK_1 | 72 | 78 | PF00454 | 0.434 |
MOD_PKA_2 | 309 | 315 | PF00069 | 0.645 |
MOD_PKA_2 | 358 | 364 | PF00069 | 0.588 |
MOD_Plk_1 | 192 | 198 | PF00069 | 0.407 |
MOD_Plk_1 | 231 | 237 | PF00069 | 0.491 |
MOD_Plk_2-3 | 193 | 199 | PF00069 | 0.324 |
MOD_Plk_4 | 101 | 107 | PF00069 | 0.232 |
MOD_Plk_4 | 148 | 154 | PF00069 | 0.597 |
MOD_Plk_4 | 200 | 206 | PF00069 | 0.304 |
MOD_Plk_4 | 433 | 439 | PF00069 | 0.657 |
MOD_Plk_4 | 69 | 75 | PF00069 | 0.417 |
MOD_Plk_4 | 88 | 94 | PF00069 | 0.187 |
MOD_ProDKin_1 | 1 | 7 | PF00069 | 0.400 |
MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.687 |
MOD_ProDKin_1 | 438 | 444 | PF00069 | 0.743 |
MOD_ProDKin_1 | 451 | 457 | PF00069 | 0.693 |
MOD_ProDKin_1 | 516 | 522 | PF00069 | 0.766 |
MOD_SUMO_rev_2 | 232 | 241 | PF00179 | 0.555 |
TRG_DiLeu_BaEn_1 | 88 | 93 | PF01217 | 0.289 |
TRG_DiLeu_BaLyEn_6 | 281 | 286 | PF01217 | 0.289 |
TRG_ENDOCYTIC_2 | 38 | 41 | PF00928 | 0.425 |
TRG_ENDOCYTIC_2 | 380 | 383 | PF00928 | 0.614 |
TRG_ER_diArg_1 | 117 | 120 | PF00400 | 0.532 |
TRG_ER_diArg_1 | 292 | 294 | PF00400 | 0.550 |
TRG_ER_diArg_1 | 309 | 311 | PF00400 | 0.702 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PFR8 | Leptomonas seymouri | 56% | 96% |
A0A1X0P4X1 | Trypanosomatidae | 39% | 100% |
A0A3S7XA08 | Leishmania donovani | 91% | 95% |
A0A422P166 | Trypanosoma rangeli | 38% | 100% |
A4HNC5 | Leishmania braziliensis | 76% | 95% |
A4IBZ8 | Leishmania infantum | 91% | 95% |
C9ZYK6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9B6Y7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 95% |
V5BT14 | Trypanosoma cruzi | 39% | 100% |