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: 4 |
NetGPI | no | yes: 0, no: 4 |
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: A4HHH0
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 | 19 | 21 | PF00675 | 0.789 |
CLV_NRD_NRD_1 | 254 | 256 | PF00675 | 0.799 |
CLV_PCSK_KEX2_1 | 253 | 255 | PF00082 | 0.814 |
CLV_PCSK_SKI1_1 | 329 | 333 | PF00082 | 0.760 |
CLV_PCSK_SKI1_1 | 8 | 12 | PF00082 | 0.750 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.603 |
DEG_SPOP_SBC_1 | 90 | 94 | PF00917 | 0.586 |
DOC_ANK_TNKS_1 | 118 | 125 | PF00023 | 0.650 |
DOC_MAPK_gen_1 | 153 | 163 | PF00069 | 0.645 |
DOC_MAPK_gen_1 | 37 | 45 | PF00069 | 0.540 |
DOC_MAPK_MEF2A_6 | 156 | 165 | PF00069 | 0.643 |
DOC_PP4_FxxP_1 | 345 | 348 | PF00568 | 0.758 |
DOC_USP7_MATH_1 | 128 | 132 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 16 | 20 | PF00917 | 0.769 |
DOC_USP7_MATH_1 | 192 | 196 | PF00917 | 0.491 |
DOC_USP7_MATH_1 | 206 | 210 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 220 | 224 | PF00917 | 0.732 |
DOC_USP7_MATH_1 | 239 | 243 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 263 | 267 | PF00917 | 0.810 |
DOC_USP7_MATH_1 | 276 | 280 | PF00917 | 0.610 |
DOC_USP7_MATH_1 | 327 | 331 | PF00917 | 0.701 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.604 |
DOC_WW_Pin1_4 | 200 | 205 | PF00397 | 0.542 |
DOC_WW_Pin1_4 | 209 | 214 | PF00397 | 0.811 |
DOC_WW_Pin1_4 | 279 | 284 | PF00397 | 0.580 |
DOC_WW_Pin1_4 | 331 | 336 | PF00397 | 0.741 |
DOC_WW_Pin1_4 | 346 | 351 | PF00397 | 0.487 |
DOC_WW_Pin1_4 | 97 | 102 | PF00397 | 0.807 |
LIG_14-3-3_CanoR_1 | 125 | 133 | PF00244 | 0.631 |
LIG_14-3-3_CanoR_1 | 197 | 202 | PF00244 | 0.634 |
LIG_14-3-3_CanoR_1 | 238 | 247 | PF00244 | 0.561 |
LIG_14-3-3_CanoR_1 | 254 | 260 | PF00244 | 0.512 |
LIG_14-3-3_CanoR_1 | 268 | 275 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 66 | 71 | PF00244 | 0.610 |
LIG_BRCT_BRCA1_1 | 92 | 96 | PF00533 | 0.731 |
LIG_deltaCOP1_diTrp_1 | 291 | 300 | PF00928 | 0.663 |
LIG_FHA_1 | 134 | 140 | PF00498 | 0.598 |
LIG_FHA_1 | 142 | 148 | PF00498 | 0.505 |
LIG_FHA_1 | 178 | 184 | PF00498 | 0.442 |
LIG_FHA_1 | 280 | 286 | PF00498 | 0.575 |
LIG_FHA_1 | 304 | 310 | PF00498 | 0.583 |
LIG_FHA_2 | 127 | 133 | PF00498 | 0.627 |
LIG_Integrin_RGD_1 | 40 | 42 | PF01839 | 0.528 |
LIG_LIR_Gen_1 | 366 | 374 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 366 | 372 | PF02991 | 0.516 |
LIG_PDZ_Class_2 | 369 | 374 | PF00595 | 0.756 |
LIG_SH2_CRK | 2 | 6 | PF00017 | 0.765 |
LIG_SH2_CRK | 369 | 373 | PF00017 | 0.518 |
LIG_SH2_NCK_1 | 275 | 279 | PF00017 | 0.594 |
LIG_SH2_NCK_1 | 28 | 32 | PF00017 | 0.701 |
LIG_SH2_PTP2 | 371 | 374 | PF00017 | 0.767 |
LIG_SH2_SRC | 275 | 278 | PF00017 | 0.828 |
LIG_SH2_STAP1 | 28 | 32 | PF00017 | 0.701 |
LIG_SH2_STAT5 | 371 | 374 | PF00017 | 0.767 |
LIG_SH3_3 | 1 | 7 | PF00018 | 0.823 |
LIG_SH3_3 | 198 | 204 | PF00018 | 0.517 |
LIG_SH3_3 | 27 | 33 | PF00018 | 0.708 |
LIG_SUMO_SIM_anti_2 | 42 | 47 | PF11976 | 0.688 |
LIG_SUMO_SIM_par_1 | 44 | 50 | PF11976 | 0.487 |
LIG_SUMO_SIM_par_1 | 66 | 72 | PF11976 | 0.596 |
LIG_SUMO_SIM_par_1 | 9 | 14 | PF11976 | 0.746 |
MOD_CDC14_SPxK_1 | 349 | 352 | PF00782 | 0.760 |
MOD_CDK_SPK_2 | 331 | 336 | PF00069 | 0.764 |
MOD_CDK_SPxK_1 | 346 | 352 | PF00069 | 0.756 |
MOD_CK1_1 | 200 | 206 | PF00069 | 0.686 |
MOD_CK1_1 | 209 | 215 | PF00069 | 0.561 |
MOD_CK1_1 | 279 | 285 | PF00069 | 0.580 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.701 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.593 |
MOD_CK2_1 | 126 | 132 | PF00069 | 0.507 |
MOD_CK2_1 | 271 | 277 | PF00069 | 0.824 |
MOD_GlcNHglycan | 12 | 16 | PF01048 | 0.747 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.620 |
MOD_GlcNHglycan | 194 | 197 | PF01048 | 0.335 |
MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.592 |
MOD_GlcNHglycan | 241 | 244 | PF01048 | 0.786 |
MOD_GlcNHglycan | 277 | 281 | PF01048 | 0.784 |
MOD_GlcNHglycan | 329 | 332 | PF01048 | 0.760 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.768 |
MOD_GlcNHglycan | 355 | 358 | PF01048 | 0.793 |
MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.677 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.813 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.501 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.629 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.610 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.354 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.691 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.694 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.741 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.541 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.720 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.505 |
MOD_N-GLC_1 | 177 | 182 | PF02516 | 0.606 |
MOD_N-GLC_2 | 351 | 353 | PF02516 | 0.534 |
MOD_NEK2_1 | 11 | 16 | PF00069 | 0.751 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.606 |
MOD_NEK2_1 | 133 | 138 | PF00069 | 0.506 |
MOD_NEK2_1 | 247 | 252 | PF00069 | 0.583 |
MOD_NEK2_2 | 177 | 182 | PF00069 | 0.606 |
MOD_PIKK_1 | 329 | 335 | PF00454 | 0.526 |
MOD_PK_1 | 197 | 203 | PF00069 | 0.494 |
MOD_PK_1 | 66 | 72 | PF00069 | 0.596 |
MOD_PKA_2 | 196 | 202 | PF00069 | 0.625 |
MOD_PKA_2 | 353 | 359 | PF00069 | 0.567 |
MOD_PKA_2 | 78 | 84 | PF00069 | 0.765 |
MOD_PKB_1 | 253 | 261 | PF00069 | 0.583 |
MOD_Plk_1 | 24 | 30 | PF00069 | 0.512 |
MOD_Plk_1 | 41 | 47 | PF00069 | 0.611 |
MOD_Plk_4 | 211 | 217 | PF00069 | 0.814 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.394 |
MOD_Plk_4 | 255 | 261 | PF00069 | 0.584 |
MOD_Plk_4 | 303 | 309 | PF00069 | 0.440 |
MOD_Plk_4 | 41 | 47 | PF00069 | 0.685 |
MOD_ProDKin_1 | 200 | 206 | PF00069 | 0.546 |
MOD_ProDKin_1 | 209 | 215 | PF00069 | 0.811 |
MOD_ProDKin_1 | 279 | 285 | PF00069 | 0.580 |
MOD_ProDKin_1 | 331 | 337 | PF00069 | 0.743 |
MOD_ProDKin_1 | 346 | 352 | PF00069 | 0.492 |
MOD_ProDKin_1 | 97 | 103 | PF00069 | 0.803 |
TRG_DiLeu_BaLyEn_6 | 122 | 127 | PF01217 | 0.650 |
TRG_ENDOCYTIC_2 | 2 | 5 | PF00928 | 0.769 |
TRG_ENDOCYTIC_2 | 369 | 372 | PF00928 | 0.722 |
TRG_ER_diArg_1 | 253 | 255 | PF00400 | 0.803 |
TRG_ER_diArg_1 | 352 | 355 | PF00400 | 0.554 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7X2H0 | Leishmania donovani | 79% | 83% |
A4I4L9 | Leishmania infantum | 79% | 83% |
E9AE17 | Leishmania major | 78% | 100% |