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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005829 | cytosol | 2 | 1 |
GO:0016020 | membrane | 2 | 1 |
GO:0019898 | extrinsic component of membrane | 2 | 1 |
GO:0034045 | phagophore assembly site membrane | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S7X2H0
Term | Name | Level | Count |
---|---|---|---|
GO:0000422 | autophagy of mitochondrion | 4 | 1 |
GO:0006497 | protein lipidation | 5 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0006914 | autophagy | 3 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007005 | mitochondrion organization | 5 | 1 |
GO:0008104 | protein localization | 4 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0022411 | cellular component disassembly | 4 | 1 |
GO:0033036 | macromolecule localization | 2 | 1 |
GO:0034497 | protein localization to phagophore assembly site | 5 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044248 | cellular catabolic process | 3 | 1 |
GO:0044804 | autophagy of nucleus | 4 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0061726 | mitochondrion disassembly | 6 | 1 |
GO:0061919 | process utilizing autophagic mechanism | 2 | 1 |
GO:0070727 | cellular macromolecule localization | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1903008 | organelle disassembly | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 1 |
GO:0005543 | phospholipid binding | 3 | 1 |
GO:0008289 | lipid binding | 2 | 1 |
GO:0032266 | phosphatidylinositol-3-phosphate binding | 6 | 1 |
GO:0035091 | phosphatidylinositol binding | 4 | 1 |
GO:0043167 | ion binding | 2 | 1 |
GO:0043168 | anion binding | 3 | 1 |
GO:0080025 | phosphatidylinositol-3,5-bisphosphate binding | 4 | 1 |
GO:1901981 | phosphatidylinositol phosphate binding | 5 | 1 |
GO:1902936 | phosphatidylinositol bisphosphate binding | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 133 | 135 | PF00675 | 0.635 |
CLV_NRD_NRD_1 | 20 | 22 | PF00675 | 0.477 |
CLV_NRD_NRD_1 | 331 | 333 | PF00675 | 0.668 |
CLV_NRD_NRD_1 | 96 | 98 | PF00675 | 0.562 |
CLV_PCSK_KEX2_1 | 133 | 135 | PF00082 | 0.661 |
CLV_PCSK_KEX2_1 | 20 | 22 | PF00082 | 0.477 |
CLV_PCSK_KEX2_1 | 331 | 333 | PF00082 | 0.670 |
CLV_PCSK_SKI1_1 | 407 | 411 | PF00082 | 0.677 |
CLV_PCSK_SKI1_1 | 85 | 89 | PF00082 | 0.462 |
DEG_SPOP_SBC_1 | 128 | 132 | PF00917 | 0.513 |
DEG_SPOP_SBC_1 | 354 | 358 | PF00917 | 0.573 |
DOC_ANK_TNKS_1 | 196 | 203 | PF00023 | 0.465 |
DOC_MAPK_gen_1 | 231 | 241 | PF00069 | 0.418 |
DOC_MAPK_MEF2A_6 | 234 | 243 | PF00069 | 0.466 |
DOC_PP4_FxxP_1 | 423 | 426 | PF00568 | 0.594 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.588 |
DOC_USP7_MATH_1 | 168 | 172 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 206 | 210 | PF00917 | 0.410 |
DOC_USP7_MATH_1 | 277 | 281 | PF00917 | 0.527 |
DOC_USP7_MATH_1 | 298 | 302 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 317 | 321 | PF00917 | 0.472 |
DOC_USP7_MATH_1 | 341 | 345 | PF00917 | 0.713 |
DOC_USP7_MATH_1 | 354 | 358 | PF00917 | 0.629 |
DOC_USP7_MATH_1 | 405 | 409 | PF00917 | 0.607 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.576 |
DOC_USP7_MATH_1 | 7 | 11 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 93 | 97 | PF00917 | 0.541 |
DOC_WW_Pin1_4 | 175 | 180 | PF00397 | 0.612 |
DOC_WW_Pin1_4 | 287 | 292 | PF00397 | 0.676 |
DOC_WW_Pin1_4 | 326 | 331 | PF00397 | 0.774 |
DOC_WW_Pin1_4 | 39 | 44 | PF00397 | 0.482 |
DOC_WW_Pin1_4 | 407 | 412 | PF00397 | 0.644 |
DOC_WW_Pin1_4 | 424 | 429 | PF00397 | 0.687 |
DOC_WW_Pin1_4 | 435 | 440 | PF00397 | 0.580 |
LIG_14-3-3_CanoR_1 | 156 | 160 | PF00244 | 0.675 |
LIG_14-3-3_CanoR_1 | 203 | 211 | PF00244 | 0.392 |
LIG_14-3-3_CanoR_1 | 278 | 284 | PF00244 | 0.596 |
LIG_14-3-3_CanoR_1 | 48 | 54 | PF00244 | 0.393 |
LIG_14-3-3_CanoR_1 | 74 | 79 | PF00244 | 0.463 |
LIG_Actin_WH2_2 | 57 | 73 | PF00022 | 0.416 |
LIG_AP_GAE_1 | 375 | 381 | PF02883 | 0.476 |
LIG_BRCT_BRCA1_1 | 170 | 174 | PF00533 | 0.663 |
LIG_deltaCOP1_diTrp_1 | 369 | 378 | PF00928 | 0.544 |
LIG_FHA_1 | 212 | 218 | PF00498 | 0.359 |
LIG_FHA_1 | 220 | 226 | PF00498 | 0.389 |
LIG_FHA_1 | 256 | 262 | PF00498 | 0.361 |
LIG_FHA_1 | 382 | 388 | PF00498 | 0.529 |
LIG_FHA_2 | 205 | 211 | PF00498 | 0.434 |
LIG_LIR_Apic_2 | 421 | 426 | PF02991 | 0.549 |
LIG_LIR_Gen_1 | 60 | 70 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 60 | 65 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 77 | 82 | PF02991 | 0.322 |
LIG_PDZ_Class_2 | 447 | 452 | PF00595 | 0.547 |
LIG_SH2_CRK | 79 | 83 | PF00017 | 0.462 |
LIG_SH2_NCK_1 | 105 | 109 | PF00017 | 0.426 |
LIG_SH2_PTP2 | 22 | 25 | PF00017 | 0.416 |
LIG_SH2_PTP2 | 449 | 452 | PF00017 | 0.541 |
LIG_SH2_SRC | 353 | 356 | PF00017 | 0.676 |
LIG_SH2_STAP1 | 105 | 109 | PF00017 | 0.436 |
LIG_SH2_STAP1 | 349 | 353 | PF00017 | 0.549 |
LIG_SH2_STAT3 | 72 | 75 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 22 | 25 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 449 | 452 | PF00017 | 0.541 |
LIG_SH2_STAT5 | 72 | 75 | PF00017 | 0.446 |
LIG_SH3_3 | 104 | 110 | PF00018 | 0.432 |
LIG_SH3_3 | 78 | 84 | PF00018 | 0.467 |
LIG_SUMO_SIM_anti_2 | 119 | 124 | PF11976 | 0.420 |
LIG_SUMO_SIM_anti_2 | 51 | 57 | PF11976 | 0.394 |
LIG_SUMO_SIM_par_1 | 63 | 69 | PF11976 | 0.431 |
LIG_SUMO_SIM_par_1 | 86 | 91 | PF11976 | 0.443 |
MOD_CDC14_SPxK_1 | 427 | 430 | PF00782 | 0.649 |
MOD_CDK_SPK_2 | 326 | 331 | PF00069 | 0.609 |
MOD_CDK_SPK_2 | 409 | 414 | PF00069 | 0.631 |
MOD_CDK_SPxK_1 | 326 | 332 | PF00069 | 0.608 |
MOD_CDK_SPxK_1 | 424 | 430 | PF00069 | 0.634 |
MOD_CDK_SPxxK_3 | 407 | 414 | PF00069 | 0.602 |
MOD_CDK_SPxxK_3 | 435 | 442 | PF00069 | 0.638 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.700 |
MOD_CK1_1 | 158 | 164 | PF00069 | 0.657 |
MOD_CK1_1 | 270 | 276 | PF00069 | 0.555 |
MOD_CK1_1 | 322 | 328 | PF00069 | 0.713 |
MOD_CK1_1 | 433 | 439 | PF00069 | 0.586 |
MOD_CK2_1 | 204 | 210 | PF00069 | 0.427 |
MOD_CK2_1 | 270 | 276 | PF00069 | 0.351 |
MOD_CK2_1 | 349 | 355 | PF00069 | 0.675 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.519 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.669 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.660 |
MOD_GlcNHglycan | 253 | 256 | PF01048 | 0.423 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.301 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.414 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.698 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.738 |
MOD_GlcNHglycan | 334 | 337 | PF01048 | 0.640 |
MOD_GlcNHglycan | 357 | 360 | PF01048 | 0.751 |
MOD_GlcNHglycan | 375 | 378 | PF01048 | 0.472 |
MOD_GlcNHglycan | 407 | 410 | PF01048 | 0.690 |
MOD_GlcNHglycan | 432 | 435 | PF01048 | 0.766 |
MOD_GlcNHglycan | 89 | 93 | PF01048 | 0.438 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.563 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.733 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.426 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.412 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.710 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.667 |
MOD_GSK3_1 | 399 | 406 | PF00069 | 0.728 |
MOD_N-GLC_1 | 166 | 171 | PF02516 | 0.596 |
MOD_N-GLC_1 | 255 | 260 | PF02516 | 0.439 |
MOD_N-GLC_1 | 347 | 352 | PF02516 | 0.621 |
MOD_N-GLC_1 | 49 | 54 | PF02516 | 0.400 |
MOD_N-GLC_1 | 7 | 12 | PF02516 | 0.519 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.608 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.416 |
MOD_NEK2_1 | 211 | 216 | PF00069 | 0.426 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.423 |
MOD_NEK2_1 | 26 | 31 | PF00069 | 0.443 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.432 |
MOD_NEK2_2 | 255 | 260 | PF00069 | 0.439 |
MOD_NEK2_2 | 418 | 423 | PF00069 | 0.521 |
MOD_OFUCOSY | 416 | 422 | PF10250 | 0.530 |
MOD_PKA_2 | 155 | 161 | PF00069 | 0.704 |
MOD_PKA_2 | 277 | 283 | PF00069 | 0.530 |
MOD_Plk_1 | 118 | 124 | PF00069 | 0.431 |
MOD_Plk_1 | 49 | 55 | PF00069 | 0.395 |
MOD_Plk_1 | 7 | 13 | PF00069 | 0.517 |
MOD_Plk_4 | 118 | 124 | PF00069 | 0.431 |
MOD_Plk_4 | 289 | 295 | PF00069 | 0.659 |
MOD_Plk_4 | 49 | 55 | PF00069 | 0.395 |
MOD_Plk_4 | 74 | 80 | PF00069 | 0.432 |
MOD_ProDKin_1 | 175 | 181 | PF00069 | 0.600 |
MOD_ProDKin_1 | 287 | 293 | PF00069 | 0.678 |
MOD_ProDKin_1 | 326 | 332 | PF00069 | 0.773 |
MOD_ProDKin_1 | 39 | 45 | PF00069 | 0.483 |
MOD_ProDKin_1 | 407 | 413 | PF00069 | 0.640 |
MOD_ProDKin_1 | 424 | 430 | PF00069 | 0.693 |
MOD_ProDKin_1 | 435 | 441 | PF00069 | 0.578 |
TRG_DiLeu_BaLyEn_6 | 200 | 205 | PF01217 | 0.447 |
TRG_ENDOCYTIC_2 | 22 | 25 | PF00928 | 0.416 |
TRG_ENDOCYTIC_2 | 449 | 452 | PF00928 | 0.530 |
TRG_ENDOCYTIC_2 | 79 | 82 | PF00928 | 0.476 |
TRG_ER_diArg_1 | 20 | 22 | PF00400 | 0.480 |
TRG_ER_diArg_1 | 330 | 332 | PF00400 | 0.665 |
TRG_Pf-PMV_PEXEL_1 | 71 | 75 | PF00026 | 0.584 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PER0 | Leptomonas seymouri | 49% | 71% |
A4HHH0 | Leishmania braziliensis | 79% | 100% |
A4I4L9 | Leishmania infantum | 100% | 100% |
C9ZLA5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
E9AE17 | Leishmania major | 94% | 100% |
E9ALR6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |