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: 5 |
NetGPI | no | yes: 0, no: 5 |
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: E9ALR6
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 | 146 | 148 | PF00675 | 0.511 |
CLV_NRD_NRD_1 | 222 | 224 | PF00675 | 0.689 |
CLV_NRD_NRD_1 | 259 | 261 | PF00675 | 0.762 |
CLV_NRD_NRD_1 | 457 | 459 | PF00675 | 0.794 |
CLV_PCSK_KEX2_1 | 146 | 148 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 259 | 261 | PF00082 | 0.817 |
CLV_PCSK_KEX2_1 | 457 | 459 | PF00082 | 0.794 |
CLV_PCSK_SKI1_1 | 211 | 215 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 533 | 537 | PF00082 | 0.807 |
DEG_SCF_FBW7_1 | 46 | 53 | PF00400 | 0.511 |
DEG_SPOP_SBC_1 | 452 | 456 | PF00917 | 0.599 |
DEG_SPOP_SBC_1 | 480 | 484 | PF00917 | 0.682 |
DEG_SPOP_SBC_1 | 96 | 100 | PF00917 | 0.597 |
DOC_ANK_TNKS_1 | 322 | 329 | PF00023 | 0.593 |
DOC_CKS1_1 | 125 | 130 | PF01111 | 0.524 |
DOC_CKS1_1 | 47 | 52 | PF01111 | 0.529 |
DOC_MAPK_gen_1 | 240 | 248 | PF00069 | 0.465 |
DOC_MAPK_gen_1 | 357 | 367 | PF00069 | 0.518 |
DOC_MAPK_gen_1 | 401 | 411 | PF00069 | 0.423 |
DOC_MAPK_gen_1 | 68 | 75 | PF00069 | 0.536 |
DOC_MAPK_MEF2A_6 | 360 | 369 | PF00069 | 0.519 |
DOC_MAPK_MEF2A_6 | 68 | 75 | PF00069 | 0.536 |
DOC_PP4_FxxP_1 | 549 | 552 | PF00568 | 0.690 |
DOC_USP7_MATH_1 | 133 | 137 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 17 | 21 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.577 |
DOC_USP7_MATH_1 | 219 | 223 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 283 | 287 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 294 | 298 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 332 | 336 | PF00917 | 0.559 |
DOC_USP7_MATH_1 | 403 | 407 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 424 | 428 | PF00917 | 0.785 |
DOC_USP7_MATH_1 | 443 | 447 | PF00917 | 0.489 |
DOC_USP7_MATH_1 | 467 | 471 | PF00917 | 0.779 |
DOC_USP7_MATH_1 | 480 | 484 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 531 | 535 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 97 | 101 | PF00917 | 0.601 |
DOC_USP7_UBL2_3 | 434 | 438 | PF12436 | 0.529 |
DOC_WW_Pin1_4 | 113 | 118 | PF00397 | 0.787 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 165 | 170 | PF00397 | 0.500 |
DOC_WW_Pin1_4 | 281 | 286 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 301 | 306 | PF00397 | 0.702 |
DOC_WW_Pin1_4 | 413 | 418 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 46 | 51 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 533 | 538 | PF00397 | 0.803 |
DOC_WW_Pin1_4 | 550 | 555 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 561 | 566 | PF00397 | 0.635 |
LIG_14-3-3_CanoR_1 | 200 | 205 | PF00244 | 0.537 |
LIG_14-3-3_CanoR_1 | 329 | 337 | PF00244 | 0.485 |
LIG_14-3-3_CanoR_1 | 404 | 410 | PF00244 | 0.593 |
LIG_Actin_WH2_2 | 183 | 199 | PF00022 | 0.494 |
LIG_AP_GAE_1 | 501 | 507 | PF02883 | 0.704 |
LIG_APCC_ABBA_1 | 409 | 414 | PF00400 | 0.489 |
LIG_BRCT_BRCA1_1 | 296 | 300 | PF00533 | 0.803 |
LIG_deltaCOP1_diTrp_1 | 495 | 504 | PF00928 | 0.729 |
LIG_FHA_1 | 338 | 344 | PF00498 | 0.461 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.500 |
LIG_FHA_1 | 382 | 388 | PF00498 | 0.505 |
LIG_FHA_1 | 508 | 514 | PF00498 | 0.636 |
LIG_FHA_1 | 51 | 57 | PF00498 | 0.449 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.599 |
LIG_FHA_2 | 125 | 131 | PF00498 | 0.514 |
LIG_FHA_2 | 331 | 337 | PF00498 | 0.482 |
LIG_FHA_2 | 80 | 86 | PF00498 | 0.636 |
LIG_Integrin_RGD_1 | 243 | 245 | PF01839 | 0.445 |
LIG_LIR_Apic_2 | 44 | 50 | PF02991 | 0.549 |
LIG_LIR_Apic_2 | 547 | 552 | PF02991 | 0.784 |
LIG_LIR_Gen_1 | 186 | 196 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 186 | 191 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 203 | 208 | PF02991 | 0.510 |
LIG_PDZ_Class_2 | 573 | 578 | PF00595 | 0.689 |
LIG_SH2_CRK | 205 | 209 | PF00017 | 0.546 |
LIG_SH2_NCK_1 | 231 | 235 | PF00017 | 0.478 |
LIG_SH2_PTP2 | 148 | 151 | PF00017 | 0.492 |
LIG_SH2_PTP2 | 575 | 578 | PF00017 | 0.786 |
LIG_SH2_SRC | 479 | 482 | PF00017 | 0.808 |
LIG_SH2_STAP1 | 231 | 235 | PF00017 | 0.486 |
LIG_SH2_STAP1 | 52 | 56 | PF00017 | 0.449 |
LIG_SH2_STAT3 | 198 | 201 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 148 | 151 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 198 | 201 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 52 | 55 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 575 | 578 | PF00017 | 0.786 |
LIG_SH3_3 | 120 | 126 | PF00018 | 0.553 |
LIG_SH3_3 | 204 | 210 | PF00018 | 0.567 |
LIG_SH3_3 | 230 | 236 | PF00018 | 0.483 |
LIG_SH3_3 | 70 | 76 | PF00018 | 0.579 |
LIG_SH3_3 | 8 | 14 | PF00018 | 0.589 |
LIG_SUMO_SIM_anti_2 | 177 | 183 | PF11976 | 0.562 |
LIG_SUMO_SIM_anti_2 | 245 | 250 | PF11976 | 0.474 |
LIG_SUMO_SIM_par_1 | 189 | 195 | PF11976 | 0.496 |
LIG_SUMO_SIM_par_1 | 212 | 217 | PF11976 | 0.495 |
MOD_CDC14_SPxK_1 | 553 | 556 | PF00782 | 0.785 |
MOD_CDK_SPK_2 | 535 | 540 | PF00069 | 0.793 |
MOD_CDK_SPxK_1 | 550 | 556 | PF00069 | 0.786 |
MOD_CDK_SPxxK_3 | 533 | 540 | PF00069 | 0.798 |
MOD_CDK_SPxxK_3 | 561 | 568 | PF00069 | 0.808 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.610 |
MOD_CK1_1 | 272 | 278 | PF00069 | 0.798 |
MOD_CK1_1 | 284 | 290 | PF00069 | 0.708 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.580 |
MOD_CK1_1 | 448 | 454 | PF00069 | 0.791 |
MOD_CK1_1 | 561 | 567 | PF00069 | 0.672 |
MOD_CK1_1 | 99 | 105 | PF00069 | 0.602 |
MOD_CK2_1 | 124 | 130 | PF00069 | 0.560 |
MOD_CK2_1 | 330 | 336 | PF00069 | 0.475 |
MOD_CK2_1 | 475 | 481 | PF00069 | 0.805 |
MOD_CK2_1 | 561 | 567 | PF00069 | 0.571 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.694 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.604 |
MOD_GlcNHglycan | 215 | 219 | PF01048 | 0.457 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.508 |
MOD_GlcNHglycan | 274 | 277 | PF01048 | 0.720 |
MOD_GlcNHglycan | 296 | 299 | PF01048 | 0.800 |
MOD_GlcNHglycan | 379 | 382 | PF01048 | 0.512 |
MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.684 |
MOD_GlcNHglycan | 445 | 448 | PF01048 | 0.772 |
MOD_GlcNHglycan | 450 | 453 | PF01048 | 0.763 |
MOD_GlcNHglycan | 460 | 463 | PF01048 | 0.581 |
MOD_GlcNHglycan | 475 | 478 | PF01048 | 0.557 |
MOD_GlcNHglycan | 483 | 486 | PF01048 | 0.738 |
MOD_GlcNHglycan | 501 | 504 | PF01048 | 0.686 |
MOD_GlcNHglycan | 533 | 536 | PF01048 | 0.809 |
MOD_GlcNHglycan | 558 | 561 | PF01048 | 0.819 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.511 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.801 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.760 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.638 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.465 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.508 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.496 |
MOD_GSK3_1 | 448 | 455 | PF00069 | 0.783 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.520 |
MOD_GSK3_1 | 475 | 482 | PF00069 | 0.804 |
MOD_GSK3_1 | 525 | 532 | PF00069 | 0.828 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.617 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.478 |
MOD_LATS_1 | 16 | 22 | PF00433 | 0.632 |
MOD_N-GLC_1 | 133 | 138 | PF02516 | 0.701 |
MOD_N-GLC_1 | 175 | 180 | PF02516 | 0.573 |
MOD_N-GLC_1 | 381 | 386 | PF02516 | 0.517 |
MOD_N-GLC_1 | 473 | 478 | PF02516 | 0.704 |
MOD_NEK2_1 | 214 | 219 | PF00069 | 0.497 |
MOD_NEK2_1 | 330 | 335 | PF00069 | 0.441 |
MOD_NEK2_1 | 337 | 342 | PF00069 | 0.476 |
MOD_NEK2_1 | 343 | 348 | PF00069 | 0.472 |
MOD_NEK2_2 | 381 | 386 | PF00069 | 0.517 |
MOD_NEK2_2 | 544 | 549 | PF00069 | 0.781 |
MOD_OFUCOSY | 542 | 548 | PF10250 | 0.778 |
MOD_PIKK_1 | 254 | 260 | PF00454 | 0.625 |
MOD_PK_1 | 18 | 24 | PF00069 | 0.636 |
MOD_PKA_2 | 17 | 23 | PF00069 | 0.558 |
MOD_PKA_2 | 272 | 278 | PF00069 | 0.789 |
MOD_PKA_2 | 403 | 409 | PF00069 | 0.574 |
MOD_PKB_1 | 556 | 564 | PF00069 | 0.538 |
MOD_Plk_1 | 133 | 139 | PF00069 | 0.689 |
MOD_Plk_1 | 175 | 181 | PF00069 | 0.584 |
MOD_Plk_1 | 244 | 250 | PF00069 | 0.474 |
MOD_Plk_4 | 175 | 181 | PF00069 | 0.584 |
MOD_Plk_4 | 200 | 206 | PF00069 | 0.494 |
MOD_Plk_4 | 244 | 250 | PF00069 | 0.474 |
MOD_Plk_4 | 415 | 421 | PF00069 | 0.721 |
MOD_Plk_4 | 7 | 13 | PF00069 | 0.588 |
MOD_ProDKin_1 | 113 | 119 | PF00069 | 0.790 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.543 |
MOD_ProDKin_1 | 165 | 171 | PF00069 | 0.497 |
MOD_ProDKin_1 | 281 | 287 | PF00069 | 0.678 |
MOD_ProDKin_1 | 301 | 307 | PF00069 | 0.690 |
MOD_ProDKin_1 | 413 | 419 | PF00069 | 0.680 |
MOD_ProDKin_1 | 46 | 52 | PF00069 | 0.538 |
MOD_ProDKin_1 | 533 | 539 | PF00069 | 0.798 |
MOD_ProDKin_1 | 550 | 556 | PF00069 | 0.510 |
MOD_ProDKin_1 | 561 | 567 | PF00069 | 0.633 |
TRG_DiLeu_BaEn_4 | 120 | 126 | PF01217 | 0.553 |
TRG_DiLeu_BaLyEn_6 | 326 | 331 | PF01217 | 0.495 |
TRG_ENDOCYTIC_2 | 148 | 151 | PF00928 | 0.492 |
TRG_ENDOCYTIC_2 | 205 | 208 | PF00928 | 0.562 |
TRG_ENDOCYTIC_2 | 575 | 578 | PF00928 | 0.786 |
TRG_ER_diArg_1 | 146 | 148 | PF00400 | 0.511 |
TRG_ER_diArg_1 | 457 | 459 | PF00400 | 0.780 |
TRG_ER_diArg_1 | 67 | 70 | PF00400 | 0.504 |
TRG_Pf-PMV_PEXEL_1 | 197 | 201 | PF00026 | 0.609 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PER0 | Leptomonas seymouri | 46% | 91% |
A0A3S7X2H0 | Leishmania donovani | 93% | 100% |
A4I4L9 | Leishmania infantum | 93% | 100% |
E9AE17 | Leishmania major | 92% | 100% |