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: 18 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0005739 | mitochondrion | 5 | 2 |
GO:0005742 | mitochondrial outer membrane translocase complex | 4 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0098796 | membrane protein complex | 2 | 2 |
GO:0098798 | mitochondrial protein-containing complex | 2 | 2 |
GO:0098799 | outer mitochondrial membrane protein complex | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: E9AFW1
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 2 |
GO:0006839 | mitochondrial transport | 4 | 2 |
GO:0006886 | intracellular protein transport | 4 | 2 |
GO:0008104 | protein localization | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0015031 | protein transport | 4 | 2 |
GO:0030150 | protein import into mitochondrial matrix | 4 | 2 |
GO:0033036 | macromolecule localization | 2 | 2 |
GO:0033365 | protein localization to organelle | 5 | 2 |
GO:0044743 | protein transmembrane import into intracellular organelle | 4 | 2 |
GO:0045184 | establishment of protein localization | 3 | 2 |
GO:0046907 | intracellular transport | 3 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0051641 | cellular localization | 2 | 2 |
GO:0051649 | establishment of localization in cell | 3 | 2 |
GO:0055085 | transmembrane transport | 2 | 2 |
GO:0065002 | intracellular protein transmembrane transport | 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:0071806 | protein transmembrane transport | 3 | 2 |
GO:0072594 | establishment of protein localization to organelle | 4 | 2 |
GO:0072655 | establishment of protein localization to mitochondrion | 5 | 2 |
GO:1990542 | mitochondrial transmembrane transport | 3 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 288 | 290 | PF00675 | 0.447 |
CLV_NRD_NRD_1 | 44 | 46 | PF00675 | 0.563 |
CLV_NRD_NRD_1 | 73 | 75 | PF00675 | 0.556 |
CLV_PCSK_KEX2_1 | 236 | 238 | PF00082 | 0.613 |
CLV_PCSK_KEX2_1 | 43 | 45 | PF00082 | 0.586 |
CLV_PCSK_PC1ET2_1 | 236 | 238 | PF00082 | 0.613 |
CLV_PCSK_PC1ET2_1 | 43 | 45 | PF00082 | 0.652 |
CLV_PCSK_SKI1_1 | 281 | 285 | PF00082 | 0.550 |
CLV_PCSK_SKI1_1 | 65 | 69 | PF00082 | 0.564 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.598 |
DEG_SCF_SKP2-CKS1_1 | 242 | 249 | PF00560 | 0.481 |
DOC_MAPK_gen_1 | 20 | 28 | PF00069 | 0.633 |
DOC_MAPK_gen_1 | 74 | 81 | PF00069 | 0.517 |
DOC_MAPK_MEF2A_6 | 309 | 316 | PF00069 | 0.439 |
DOC_MAPK_NFAT4_5 | 309 | 317 | PF00069 | 0.534 |
DOC_PP1_RVXF_1 | 325 | 331 | PF00149 | 0.559 |
DOC_PP2B_LxvP_1 | 312 | 315 | PF13499 | 0.553 |
DOC_USP7_MATH_1 | 114 | 118 | PF00917 | 0.463 |
DOC_USP7_MATH_1 | 61 | 65 | PF00917 | 0.622 |
DOC_USP7_UBL2_3 | 249 | 253 | PF12436 | 0.428 |
DOC_WW_Pin1_4 | 243 | 248 | PF00397 | 0.489 |
LIG_14-3-3_CanoR_1 | 148 | 157 | PF00244 | 0.485 |
LIG_14-3-3_CanoR_1 | 289 | 293 | PF00244 | 0.549 |
LIG_14-3-3_CanoR_1 | 327 | 331 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 7 | 16 | PF00244 | 0.632 |
LIG_Actin_WH2_2 | 313 | 329 | PF00022 | 0.619 |
LIG_FHA_1 | 249 | 255 | PF00498 | 0.496 |
LIG_FHA_1 | 297 | 303 | PF00498 | 0.467 |
LIG_FHA_1 | 91 | 97 | PF00498 | 0.466 |
LIG_FHA_2 | 255 | 261 | PF00498 | 0.399 |
LIG_LIR_Gen_1 | 106 | 116 | PF02991 | 0.600 |
LIG_LIR_Gen_1 | 135 | 144 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 106 | 112 | PF02991 | 0.580 |
LIG_LIR_Nem_3 | 135 | 139 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 68 | 72 | PF02991 | 0.465 |
LIG_PDZ_Class_2 | 344 | 349 | PF00595 | 0.400 |
LIG_SH2_CRK | 146 | 150 | PF00017 | 0.447 |
LIG_SH2_CRK | 69 | 73 | PF00017 | 0.452 |
LIG_SH2_SRC | 334 | 337 | PF00017 | 0.452 |
LIG_SH2_STAP1 | 334 | 338 | PF00017 | 0.495 |
LIG_SH2_STAP1 | 48 | 52 | PF00017 | 0.684 |
LIG_SH2_STAT5 | 191 | 194 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 225 | 228 | PF00017 | 0.519 |
LIG_SH3_1 | 57 | 63 | PF00018 | 0.530 |
LIG_SH3_2 | 60 | 65 | PF14604 | 0.541 |
LIG_SH3_3 | 57 | 63 | PF00018 | 0.520 |
LIG_TRAF2_1 | 16 | 19 | PF00917 | 0.714 |
LIG_TYR_ITIM | 144 | 149 | PF00017 | 0.424 |
LIG_TYR_ITIM | 67 | 72 | PF00017 | 0.468 |
MOD_CDK_SPxK_1 | 243 | 249 | PF00069 | 0.492 |
MOD_CK1_1 | 135 | 141 | PF00069 | 0.408 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.564 |
MOD_CK1_1 | 221 | 227 | PF00069 | 0.472 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.491 |
MOD_CK1_1 | 248 | 254 | PF00069 | 0.485 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.648 |
MOD_CK2_1 | 114 | 120 | PF00069 | 0.451 |
MOD_CK2_1 | 52 | 58 | PF00069 | 0.572 |
MOD_CK2_1 | 6 | 12 | PF00069 | 0.743 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.499 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.611 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.418 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.452 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.416 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.405 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.416 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.592 |
MOD_N-GLC_1 | 213 | 218 | PF02516 | 0.478 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.439 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.516 |
MOD_NEK2_1 | 174 | 179 | PF00069 | 0.455 |
MOD_NEK2_1 | 197 | 202 | PF00069 | 0.411 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.442 |
MOD_NEK2_1 | 298 | 303 | PF00069 | 0.475 |
MOD_NEK2_1 | 326 | 331 | PF00069 | 0.529 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.532 |
MOD_NEK2_1 | 6 | 11 | PF00069 | 0.740 |
MOD_PIKK_1 | 155 | 161 | PF00454 | 0.447 |
MOD_PIKK_1 | 166 | 172 | PF00454 | 0.379 |
MOD_PIKK_1 | 174 | 180 | PF00454 | 0.420 |
MOD_PIKK_1 | 184 | 190 | PF00454 | 0.450 |
MOD_PKA_2 | 147 | 153 | PF00069 | 0.460 |
MOD_PKA_2 | 288 | 294 | PF00069 | 0.546 |
MOD_PKA_2 | 326 | 332 | PF00069 | 0.553 |
MOD_PKA_2 | 6 | 12 | PF00069 | 0.728 |
MOD_Plk_1 | 193 | 199 | PF00069 | 0.438 |
MOD_Plk_1 | 213 | 219 | PF00069 | 0.483 |
MOD_Plk_1 | 259 | 265 | PF00069 | 0.334 |
MOD_Plk_4 | 169 | 175 | PF00069 | 0.403 |
MOD_Plk_4 | 221 | 227 | PF00069 | 0.560 |
MOD_Plk_4 | 288 | 294 | PF00069 | 0.515 |
MOD_Plk_4 | 298 | 304 | PF00069 | 0.498 |
MOD_ProDKin_1 | 243 | 249 | PF00069 | 0.492 |
MOD_SUMO_rev_2 | 12 | 22 | PF00179 | 0.732 |
MOD_SUMO_rev_2 | 46 | 53 | PF00179 | 0.589 |
TRG_DiLeu_BaLyEn_6 | 201 | 206 | PF01217 | 0.464 |
TRG_ENDOCYTIC_2 | 142 | 145 | PF00928 | 0.442 |
TRG_ENDOCYTIC_2 | 146 | 149 | PF00928 | 0.448 |
TRG_ENDOCYTIC_2 | 69 | 72 | PF00928 | 0.425 |
TRG_Pf-PMV_PEXEL_1 | 50 | 54 | PF00026 | 0.650 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PE17 | Leptomonas seymouri | 82% | 100% |
A0A0S4J3Y4 | Bodo saltans | 47% | 100% |
A0A1X0P556 | Trypanosomatidae | 55% | 100% |
A0A3R7KX50 | Trypanosoma rangeli | 54% | 100% |
A0A3S7XA15 | Leishmania donovani | 98% | 100% |
A4HNF0 | Leishmania braziliensis | 92% | 100% |
A4IC22 | Leishmania infantum | 98% | 100% |
C9ZYH7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 53% | 99% |
E9B714 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
V5D7G9 | Trypanosoma cruzi | 53% | 100% |