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: A0A3S7WRQ0
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_NRD_NRD_1 | 258 | 260 | PF00675 | 0.466 |
CLV_NRD_NRD_1 | 36 | 38 | PF00675 | 0.734 |
CLV_NRD_NRD_1 | 405 | 407 | PF00675 | 0.416 |
CLV_NRD_NRD_1 | 70 | 72 | PF00675 | 0.713 |
CLV_PCSK_KEX2_1 | 215 | 217 | PF00082 | 0.271 |
CLV_PCSK_KEX2_1 | 258 | 260 | PF00082 | 0.466 |
CLV_PCSK_KEX2_1 | 36 | 38 | PF00082 | 0.734 |
CLV_PCSK_KEX2_1 | 70 | 72 | PF00082 | 0.713 |
CLV_PCSK_PC1ET2_1 | 215 | 217 | PF00082 | 0.271 |
CLV_PCSK_SKI1_1 | 115 | 119 | PF00082 | 0.583 |
CLV_PCSK_SKI1_1 | 170 | 174 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 216 | 220 | PF00082 | 0.276 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.267 |
CLV_PCSK_SKI1_1 | 239 | 243 | PF00082 | 0.264 |
CLV_PCSK_SKI1_1 | 276 | 280 | PF00082 | 0.499 |
CLV_PCSK_SKI1_1 | 363 | 367 | PF00082 | 0.352 |
CLV_Separin_Metazoa | 140 | 144 | PF03568 | 0.367 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.536 |
DOC_CDC14_PxL_1 | 172 | 180 | PF14671 | 0.386 |
DOC_CDC14_PxL_1 | 267 | 275 | PF14671 | 0.283 |
DOC_CKS1_1 | 245 | 250 | PF01111 | 0.386 |
DOC_CKS1_1 | 25 | 30 | PF01111 | 0.464 |
DOC_CYCLIN_RxL_1 | 167 | 177 | PF00134 | 0.449 |
DOC_CYCLIN_yCln2_LP_2 | 351 | 357 | PF00134 | 0.344 |
DOC_MAPK_FxFP_2 | 366 | 369 | PF00069 | 0.562 |
DOC_MAPK_gen_1 | 143 | 153 | PF00069 | 0.383 |
DOC_MAPK_gen_1 | 307 | 317 | PF00069 | 0.476 |
DOC_MAPK_gen_1 | 53 | 63 | PF00069 | 0.503 |
DOC_MAPK_MEF2A_6 | 322 | 331 | PF00069 | 0.386 |
DOC_MAPK_MEF2A_6 | 56 | 65 | PF00069 | 0.501 |
DOC_PP1_RVXF_1 | 68 | 75 | PF00149 | 0.437 |
DOC_PP2B_LxvP_1 | 278 | 281 | PF13499 | 0.276 |
DOC_PP4_FxxP_1 | 131 | 134 | PF00568 | 0.362 |
DOC_PP4_FxxP_1 | 245 | 248 | PF00568 | 0.406 |
DOC_PP4_FxxP_1 | 366 | 369 | PF00568 | 0.550 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.387 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 374 | 378 | PF00917 | 0.649 |
DOC_USP7_UBL2_3 | 215 | 219 | PF12436 | 0.476 |
DOC_WW_Pin1_4 | 24 | 29 | PF00397 | 0.531 |
DOC_WW_Pin1_4 | 244 | 249 | PF00397 | 0.386 |
LIG_14-3-3_CanoR_1 | 170 | 175 | PF00244 | 0.329 |
LIG_14-3-3_CanoR_1 | 182 | 186 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 208 | 218 | PF00244 | 0.490 |
LIG_14-3-3_CanoR_1 | 307 | 317 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 322 | 327 | PF00244 | 0.329 |
LIG_14-3-3_CanoR_1 | 410 | 418 | PF00244 | 0.694 |
LIG_14-3-3_CanoR_1 | 56 | 63 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 70 | 75 | PF00244 | 0.388 |
LIG_AP2alpha_1 | 362 | 366 | PF02296 | 0.565 |
LIG_BRCT_BRCA1_1 | 336 | 340 | PF00533 | 0.287 |
LIG_Clathr_ClatBox_1 | 296 | 300 | PF01394 | 0.363 |
LIG_deltaCOP1_diTrp_1 | 122 | 131 | PF00928 | 0.354 |
LIG_EVH1_1 | 368 | 372 | PF00568 | 0.555 |
LIG_FHA_1 | 15 | 21 | PF00498 | 0.558 |
LIG_FHA_1 | 244 | 250 | PF00498 | 0.322 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.276 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.344 |
LIG_FHA_2 | 263 | 269 | PF00498 | 0.294 |
LIG_FHA_2 | 277 | 283 | PF00498 | 0.225 |
LIG_FHA_2 | 393 | 399 | PF00498 | 0.652 |
LIG_FHA_2 | 418 | 424 | PF00498 | 0.700 |
LIG_LIR_Apic_2 | 108 | 113 | PF02991 | 0.412 |
LIG_LIR_Apic_2 | 130 | 134 | PF02991 | 0.372 |
LIG_LIR_Apic_2 | 243 | 248 | PF02991 | 0.406 |
LIG_LIR_Apic_2 | 282 | 288 | PF02991 | 0.275 |
LIG_LIR_Apic_2 | 364 | 369 | PF02991 | 0.566 |
LIG_LIR_Gen_1 | 116 | 124 | PF02991 | 0.360 |
LIG_LIR_Gen_1 | 148 | 155 | PF02991 | 0.463 |
LIG_LIR_Gen_1 | 220 | 229 | PF02991 | 0.487 |
LIG_LIR_Gen_1 | 252 | 262 | PF02991 | 0.367 |
LIG_LIR_Gen_1 | 387 | 394 | PF02991 | 0.688 |
LIG_LIR_Gen_1 | 42 | 47 | PF02991 | 0.572 |
LIG_LIR_Gen_1 | 422 | 432 | PF02991 | 0.681 |
LIG_LIR_Nem_3 | 116 | 121 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 148 | 153 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 236 | 241 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 252 | 257 | PF02991 | 0.228 |
LIG_LIR_Nem_3 | 364 | 368 | PF02991 | 0.563 |
LIG_LIR_Nem_3 | 387 | 392 | PF02991 | 0.693 |
LIG_LIR_Nem_3 | 42 | 46 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 422 | 427 | PF02991 | 0.648 |
LIG_LIR_Nem_3 | 73 | 77 | PF02991 | 0.505 |
LIG_NRP_CendR_1 | 440 | 441 | PF00754 | 0.611 |
LIG_Pex14_1 | 127 | 131 | PF04695 | 0.379 |
LIG_Pex14_1 | 158 | 162 | PF04695 | 0.276 |
LIG_Pex14_2 | 241 | 245 | PF04695 | 0.406 |
LIG_Pex14_2 | 295 | 299 | PF04695 | 0.329 |
LIG_Pex14_2 | 362 | 366 | PF04695 | 0.540 |
LIG_SH2_CRK | 285 | 289 | PF00017 | 0.363 |
LIG_SH2_NCK_1 | 285 | 289 | PF00017 | 0.476 |
LIG_SH2_NCK_1 | 424 | 428 | PF00017 | 0.715 |
LIG_SH2_PTP2 | 110 | 113 | PF00017 | 0.476 |
LIG_SH2_STAP1 | 263 | 267 | PF00017 | 0.276 |
LIG_SH2_STAP1 | 389 | 393 | PF00017 | 0.696 |
LIG_SH2_STAP1 | 424 | 428 | PF00017 | 0.653 |
LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 316 | 319 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 330 | 333 | PF00017 | 0.328 |
LIG_SH3_3 | 22 | 28 | PF00018 | 0.463 |
LIG_SH3_3 | 366 | 372 | PF00018 | 0.560 |
LIG_SUMO_SIM_par_1 | 103 | 109 | PF11976 | 0.461 |
LIG_SxIP_EBH_1 | 168 | 182 | PF03271 | 0.363 |
LIG_TRAF2_1 | 394 | 397 | PF00917 | 0.572 |
LIG_UBA3_1 | 379 | 384 | PF00899 | 0.670 |
LIG_WRC_WIRS_1 | 150 | 155 | PF05994 | 0.400 |
LIG_WRC_WIRS_1 | 242 | 247 | PF05994 | 0.292 |
MOD_CDK_SPxxK_3 | 24 | 31 | PF00069 | 0.467 |
MOD_CK1_1 | 177 | 183 | PF00069 | 0.476 |
MOD_CK1_1 | 195 | 201 | PF00069 | 0.397 |
MOD_CK1_1 | 240 | 246 | PF00069 | 0.347 |
MOD_CK2_1 | 113 | 119 | PF00069 | 0.381 |
MOD_CK2_1 | 208 | 214 | PF00069 | 0.476 |
MOD_CK2_1 | 262 | 268 | PF00069 | 0.278 |
MOD_CK2_1 | 384 | 390 | PF00069 | 0.611 |
MOD_CK2_1 | 392 | 398 | PF00069 | 0.594 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.698 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.317 |
MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.329 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.305 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.490 |
MOD_GlcNHglycan | 413 | 416 | PF01048 | 0.497 |
MOD_GlcNHglycan | 436 | 439 | PF01048 | 0.563 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.703 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.329 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.522 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.276 |
MOD_GSK3_1 | 374 | 381 | PF00069 | 0.639 |
MOD_N-GLC_1 | 233 | 238 | PF02516 | 0.289 |
MOD_NEK2_1 | 19 | 24 | PF00069 | 0.541 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.532 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.384 |
MOD_NEK2_2 | 113 | 118 | PF00069 | 0.396 |
MOD_NEK2_2 | 253 | 258 | PF00069 | 0.329 |
MOD_PIKK_1 | 233 | 239 | PF00454 | 0.516 |
MOD_PIKK_1 | 392 | 398 | PF00454 | 0.624 |
MOD_PK_1 | 31 | 37 | PF00069 | 0.414 |
MOD_PK_1 | 322 | 328 | PF00069 | 0.406 |
MOD_PKA_1 | 70 | 76 | PF00069 | 0.426 |
MOD_PKA_2 | 181 | 187 | PF00069 | 0.513 |
MOD_PKA_2 | 321 | 327 | PF00069 | 0.414 |
MOD_PKA_2 | 55 | 61 | PF00069 | 0.539 |
MOD_PKA_2 | 70 | 76 | PF00069 | 0.488 |
MOD_PKA_2 | 85 | 91 | PF00069 | 0.436 |
MOD_Plk_1 | 113 | 119 | PF00069 | 0.381 |
MOD_Plk_1 | 206 | 212 | PF00069 | 0.476 |
MOD_Plk_1 | 233 | 239 | PF00069 | 0.489 |
MOD_Plk_1 | 276 | 282 | PF00069 | 0.281 |
MOD_Plk_1 | 397 | 403 | PF00069 | 0.682 |
MOD_Plk_4 | 113 | 119 | PF00069 | 0.392 |
MOD_Plk_4 | 127 | 133 | PF00069 | 0.382 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.335 |
MOD_Plk_4 | 237 | 243 | PF00069 | 0.489 |
MOD_Plk_4 | 322 | 328 | PF00069 | 0.362 |
MOD_Plk_4 | 384 | 390 | PF00069 | 0.617 |
MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.533 |
MOD_ProDKin_1 | 244 | 250 | PF00069 | 0.386 |
MOD_SUMO_rev_2 | 377 | 386 | PF00179 | 0.672 |
TRG_DiLeu_BaEn_2 | 267 | 273 | PF01217 | 0.276 |
TRG_DiLeu_BaEn_4 | 397 | 403 | PF01217 | 0.665 |
TRG_DiLeu_BaLyEn_6 | 28 | 33 | PF01217 | 0.448 |
TRG_ENDOCYTIC_2 | 222 | 225 | PF00928 | 0.487 |
TRG_ENDOCYTIC_2 | 389 | 392 | PF00928 | 0.697 |
TRG_ENDOCYTIC_2 | 424 | 427 | PF00928 | 0.652 |
TRG_ER_diArg_1 | 257 | 259 | PF00400 | 0.267 |
TRG_ER_diArg_1 | 35 | 37 | PF00400 | 0.568 |
TRG_ER_diArg_1 | 70 | 72 | PF00400 | 0.531 |
TRG_Pf-PMV_PEXEL_1 | 115 | 119 | PF00026 | 0.657 |
TRG_Pf-PMV_PEXEL_1 | 143 | 148 | PF00026 | 0.572 |
TRG_Pf-PMV_PEXEL_1 | 216 | 220 | PF00026 | 0.287 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2Y9 | Leptomonas seymouri | 84% | 98% |
A0A0S4IZY1 | Bodo saltans | 62% | 100% |
A0A1X0NWK5 | Trypanosomatidae | 70% | 100% |
A0A3R7NUU3 | Trypanosoma rangeli | 71% | 99% |
A4H6P4 | Leishmania braziliensis | 90% | 100% |
A4HV25 | Leishmania infantum | 100% | 100% |
D0A7C4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 62% | 100% |
E9ANQ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
Q4QGW4 | Leishmania major | 97% | 100% |
V5C1D0 | Trypanosoma cruzi | 67% | 100% |