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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
Related structures:
AlphaFold database: E9ANQ7
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 | 12 |
GO:0140104 | molecular carrier activity | 1 | 12 |
GO:0140597 | protein carrier chaperone | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 423 | 427 | PF00656 | 0.570 |
CLV_NRD_NRD_1 | 262 | 264 | PF00675 | 0.455 |
CLV_NRD_NRD_1 | 409 | 411 | PF00675 | 0.452 |
CLV_PCSK_KEX2_1 | 219 | 221 | PF00082 | 0.255 |
CLV_PCSK_KEX2_1 | 262 | 264 | PF00082 | 0.455 |
CLV_PCSK_PC1ET2_1 | 219 | 221 | PF00082 | 0.255 |
CLV_PCSK_SKI1_1 | 119 | 123 | PF00082 | 0.558 |
CLV_PCSK_SKI1_1 | 174 | 178 | PF00082 | 0.329 |
CLV_PCSK_SKI1_1 | 220 | 224 | PF00082 | 0.255 |
CLV_PCSK_SKI1_1 | 230 | 234 | PF00082 | 0.255 |
CLV_PCSK_SKI1_1 | 243 | 247 | PF00082 | 0.271 |
CLV_PCSK_SKI1_1 | 280 | 284 | PF00082 | 0.480 |
CLV_PCSK_SKI1_1 | 367 | 371 | PF00082 | 0.337 |
CLV_Separin_Metazoa | 144 | 148 | PF03568 | 0.348 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.524 |
DOC_CDC14_PxL_1 | 176 | 184 | PF14671 | 0.358 |
DOC_CDC14_PxL_1 | 271 | 279 | PF14671 | 0.266 |
DOC_CKS1_1 | 25 | 30 | PF01111 | 0.453 |
DOC_CYCLIN_RxL_1 | 171 | 181 | PF00134 | 0.433 |
DOC_CYCLIN_yCln2_LP_2 | 355 | 361 | PF00134 | 0.314 |
DOC_MAPK_FxFP_2 | 370 | 373 | PF00069 | 0.548 |
DOC_MAPK_gen_1 | 147 | 157 | PF00069 | 0.376 |
DOC_MAPK_gen_1 | 311 | 321 | PF00069 | 0.455 |
DOC_MAPK_gen_1 | 57 | 67 | PF00069 | 0.471 |
DOC_MAPK_MEF2A_6 | 326 | 335 | PF00069 | 0.358 |
DOC_MAPK_MEF2A_6 | 60 | 69 | PF00069 | 0.470 |
DOC_MIT_MIM_1 | 168 | 178 | PF04212 | 0.265 |
DOC_PP1_RVXF_1 | 72 | 79 | PF00149 | 0.425 |
DOC_PP2B_LxvP_1 | 282 | 285 | PF13499 | 0.262 |
DOC_PP4_FxxP_1 | 135 | 138 | PF00568 | 0.346 |
DOC_PP4_FxxP_1 | 249 | 252 | PF00568 | 0.382 |
DOC_PP4_FxxP_1 | 370 | 373 | PF00568 | 0.537 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.370 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.491 |
DOC_USP7_MATH_1 | 378 | 382 | PF00917 | 0.630 |
DOC_USP7_UBL2_3 | 219 | 223 | PF12436 | 0.455 |
DOC_WW_Pin1_4 | 24 | 29 | PF00397 | 0.524 |
LIG_14-3-3_CanoR_1 | 174 | 179 | PF00244 | 0.299 |
LIG_14-3-3_CanoR_1 | 186 | 190 | PF00244 | 0.455 |
LIG_14-3-3_CanoR_1 | 212 | 222 | PF00244 | 0.469 |
LIG_14-3-3_CanoR_1 | 31 | 41 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 311 | 321 | PF00244 | 0.455 |
LIG_14-3-3_CanoR_1 | 326 | 331 | PF00244 | 0.390 |
LIG_14-3-3_CanoR_1 | 414 | 422 | PF00244 | 0.674 |
LIG_14-3-3_CanoR_1 | 60 | 67 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 74 | 79 | PF00244 | 0.378 |
LIG_AP2alpha_1 | 366 | 370 | PF02296 | 0.550 |
LIG_BRCT_BRCA1_1 | 340 | 344 | PF00533 | 0.266 |
LIG_BRCT_BRCA1_1 | 43 | 47 | PF00533 | 0.404 |
LIG_Clathr_ClatBox_1 | 300 | 304 | PF01394 | 0.334 |
LIG_deltaCOP1_diTrp_1 | 126 | 135 | PF00928 | 0.339 |
LIG_EVH1_1 | 372 | 376 | PF00568 | 0.543 |
LIG_FHA_1 | 15 | 21 | PF00498 | 0.444 |
LIG_FHA_1 | 248 | 254 | PF00498 | 0.299 |
LIG_FHA_1 | 286 | 292 | PF00498 | 0.255 |
LIG_FHA_1 | 350 | 356 | PF00498 | 0.314 |
LIG_FHA_2 | 107 | 113 | PF00498 | 0.467 |
LIG_FHA_2 | 267 | 273 | PF00498 | 0.271 |
LIG_FHA_2 | 281 | 287 | PF00498 | 0.230 |
LIG_FHA_2 | 397 | 403 | PF00498 | 0.634 |
LIG_LIR_Apic_2 | 112 | 117 | PF02991 | 0.400 |
LIG_LIR_Apic_2 | 134 | 138 | PF02991 | 0.358 |
LIG_LIR_Apic_2 | 247 | 252 | PF02991 | 0.382 |
LIG_LIR_Apic_2 | 286 | 292 | PF02991 | 0.255 |
LIG_LIR_Apic_2 | 368 | 373 | PF02991 | 0.551 |
LIG_LIR_Gen_1 | 120 | 128 | PF02991 | 0.335 |
LIG_LIR_Gen_1 | 152 | 159 | PF02991 | 0.423 |
LIG_LIR_Gen_1 | 224 | 233 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 256 | 266 | PF02991 | 0.346 |
LIG_LIR_Gen_1 | 391 | 398 | PF02991 | 0.678 |
LIG_LIR_Gen_1 | 42 | 51 | PF02991 | 0.470 |
LIG_LIR_Gen_1 | 426 | 436 | PF02991 | 0.631 |
LIG_LIR_Nem_3 | 120 | 125 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 152 | 157 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 240 | 245 | PF02991 | 0.584 |
LIG_LIR_Nem_3 | 256 | 261 | PF02991 | 0.290 |
LIG_LIR_Nem_3 | 368 | 372 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 391 | 396 | PF02991 | 0.684 |
LIG_LIR_Nem_3 | 42 | 46 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 426 | 431 | PF02991 | 0.622 |
LIG_LIR_Nem_3 | 77 | 81 | PF02991 | 0.491 |
LIG_NRP_CendR_1 | 444 | 445 | PF00754 | 0.555 |
LIG_Pex14_1 | 131 | 135 | PF04695 | 0.364 |
LIG_Pex14_1 | 162 | 166 | PF04695 | 0.255 |
LIG_Pex14_2 | 245 | 249 | PF04695 | 0.382 |
LIG_Pex14_2 | 299 | 303 | PF04695 | 0.299 |
LIG_Pex14_2 | 366 | 370 | PF04695 | 0.525 |
LIG_Pex14_2 | 43 | 47 | PF04695 | 0.443 |
LIG_SH2_CRK | 289 | 293 | PF00017 | 0.334 |
LIG_SH2_NCK_1 | 289 | 293 | PF00017 | 0.419 |
LIG_SH2_NCK_1 | 428 | 432 | PF00017 | 0.682 |
LIG_SH2_PTP2 | 114 | 117 | PF00017 | 0.463 |
LIG_SH2_STAP1 | 267 | 271 | PF00017 | 0.255 |
LIG_SH2_STAP1 | 393 | 397 | PF00017 | 0.682 |
LIG_SH2_STAP1 | 428 | 432 | PF00017 | 0.615 |
LIG_SH2_STAT5 | 114 | 117 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 320 | 323 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 334 | 337 | PF00017 | 0.351 |
LIG_SH3_3 | 22 | 28 | PF00018 | 0.476 |
LIG_SH3_3 | 370 | 376 | PF00018 | 0.545 |
LIG_SxIP_EBH_1 | 172 | 186 | PF03271 | 0.334 |
LIG_TRAF2_1 | 398 | 401 | PF00917 | 0.566 |
LIG_UBA3_1 | 383 | 388 | PF00899 | 0.635 |
LIG_WRC_WIRS_1 | 154 | 159 | PF05994 | 0.372 |
LIG_WRC_WIRS_1 | 246 | 251 | PF05994 | 0.266 |
MOD_CDK_SPxxK_3 | 24 | 31 | PF00069 | 0.453 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.418 |
MOD_CK1_1 | 181 | 187 | PF00069 | 0.467 |
MOD_CK1_1 | 199 | 205 | PF00069 | 0.467 |
MOD_CK1_1 | 244 | 250 | PF00069 | 0.317 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.425 |
MOD_CK2_1 | 117 | 123 | PF00069 | 0.365 |
MOD_CK2_1 | 212 | 218 | PF00069 | 0.460 |
MOD_CK2_1 | 266 | 272 | PF00069 | 0.258 |
MOD_CK2_1 | 388 | 394 | PF00069 | 0.595 |
MOD_CK2_1 | 396 | 402 | PF00069 | 0.590 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.712 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.297 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.299 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.296 |
MOD_GlcNHglycan | 340 | 343 | PF01048 | 0.468 |
MOD_GlcNHglycan | 417 | 420 | PF01048 | 0.449 |
MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.750 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.710 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.419 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.299 |
MOD_GSK3_1 | 237 | 244 | PF00069 | 0.591 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.301 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.621 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.455 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.483 |
MOD_NEK2_1 | 19 | 24 | PF00069 | 0.539 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.522 |
MOD_NEK2_1 | 245 | 250 | PF00069 | 0.343 |
MOD_NEK2_1 | 46 | 51 | PF00069 | 0.486 |
MOD_NEK2_2 | 117 | 122 | PF00069 | 0.375 |
MOD_NEK2_2 | 257 | 262 | PF00069 | 0.299 |
MOD_PIKK_1 | 237 | 243 | PF00454 | 0.486 |
MOD_PIKK_1 | 396 | 402 | PF00454 | 0.646 |
MOD_PKA_2 | 185 | 191 | PF00069 | 0.490 |
MOD_PKA_2 | 325 | 331 | PF00069 | 0.433 |
MOD_PKA_2 | 59 | 65 | PF00069 | 0.514 |
MOD_PKA_2 | 89 | 95 | PF00069 | 0.428 |
MOD_Plk_1 | 117 | 123 | PF00069 | 0.359 |
MOD_Plk_1 | 210 | 216 | PF00069 | 0.455 |
MOD_Plk_1 | 280 | 286 | PF00069 | 0.259 |
MOD_Plk_1 | 401 | 407 | PF00069 | 0.642 |
MOD_Plk_4 | 117 | 123 | PF00069 | 0.370 |
MOD_Plk_4 | 131 | 137 | PF00069 | 0.356 |
MOD_Plk_4 | 15 | 21 | PF00069 | 0.374 |
MOD_Plk_4 | 174 | 180 | PF00069 | 0.305 |
MOD_Plk_4 | 241 | 247 | PF00069 | 0.476 |
MOD_Plk_4 | 326 | 332 | PF00069 | 0.334 |
MOD_Plk_4 | 388 | 394 | PF00069 | 0.592 |
MOD_Plk_4 | 42 | 48 | PF00069 | 0.376 |
MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.527 |
MOD_SUMO_rev_2 | 381 | 390 | PF00179 | 0.644 |
TRG_DiLeu_BaEn_2 | 271 | 277 | PF01217 | 0.255 |
TRG_DiLeu_BaEn_4 | 401 | 407 | PF01217 | 0.625 |
TRG_DiLeu_BaLyEn_6 | 171 | 176 | PF01217 | 0.265 |
TRG_ENDOCYTIC_2 | 226 | 229 | PF00928 | 0.466 |
TRG_ENDOCYTIC_2 | 393 | 396 | PF00928 | 0.683 |
TRG_ENDOCYTIC_2 | 428 | 431 | PF00928 | 0.614 |
TRG_ER_diArg_1 | 261 | 263 | PF00400 | 0.255 |
TRG_NLS_Bipartite_1 | 219 | 239 | PF00514 | 0.421 |
TRG_Pf-PMV_PEXEL_1 | 119 | 123 | PF00026 | 0.643 |
TRG_Pf-PMV_PEXEL_1 | 147 | 152 | PF00026 | 0.552 |
TRG_Pf-PMV_PEXEL_1 | 220 | 224 | PF00026 | 0.266 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2Y9 | Leptomonas seymouri | 85% | 99% |
A0A0S4IZY1 | Bodo saltans | 61% | 100% |
A0A1X0NWK5 | Trypanosomatidae | 71% | 100% |
A0A3R7NUU3 | Trypanosoma rangeli | 71% | 100% |
A0A3S7WRQ0 | Leishmania donovani | 94% | 100% |
A4H6P4 | Leishmania braziliensis | 89% | 100% |
A4HV25 | Leishmania infantum | 94% | 100% |
D0A7C4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 62% | 100% |
Q4QGW4 | Leishmania major | 95% | 100% |
V5C1D0 | Trypanosoma cruzi | 75% | 100% |