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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005739 | mitochondrion | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AJ91
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 6 |
GO:0008152 | metabolic process | 1 | 6 |
GO:0009056 | catabolic process | 2 | 6 |
GO:0016042 | lipid catabolic process | 4 | 6 |
GO:0044238 | primary metabolic process | 2 | 6 |
GO:0071704 | organic substance metabolic process | 2 | 6 |
GO:1901575 | organic substance catabolic process | 3 | 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 8 |
GO:0003824 | catalytic activity | 1 | 8 |
GO:0004658 | propionyl-CoA carboxylase activity | 5 | 6 |
GO:0005488 | binding | 1 | 8 |
GO:0005524 | ATP binding | 5 | 8 |
GO:0016421 | CoA carboxylase activity | 4 | 6 |
GO:0016874 | ligase activity | 2 | 8 |
GO:0016885 | ligase activity, forming carbon-carbon bonds | 3 | 6 |
GO:0017076 | purine nucleotide binding | 4 | 8 |
GO:0030554 | adenyl nucleotide binding | 5 | 8 |
GO:0032553 | ribonucleotide binding | 3 | 8 |
GO:0032555 | purine ribonucleotide binding | 4 | 8 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 8 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 8 |
GO:0036094 | small molecule binding | 2 | 8 |
GO:0043167 | ion binding | 2 | 8 |
GO:0043168 | anion binding | 3 | 8 |
GO:0043169 | cation binding | 3 | 8 |
GO:0046872 | metal ion binding | 4 | 8 |
GO:0097159 | organic cyclic compound binding | 2 | 8 |
GO:0097367 | carbohydrate derivative binding | 2 | 8 |
GO:1901265 | nucleoside phosphate binding | 3 | 8 |
GO:1901363 | heterocyclic compound binding | 2 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 221 | 223 | PF00675 | 0.274 |
CLV_NRD_NRD_1 | 237 | 239 | PF00675 | 0.223 |
CLV_NRD_NRD_1 | 255 | 257 | PF00675 | 0.221 |
CLV_PCSK_KEX2_1 | 124 | 126 | PF00082 | 0.263 |
CLV_PCSK_KEX2_1 | 221 | 223 | PF00082 | 0.236 |
CLV_PCSK_KEX2_1 | 237 | 239 | PF00082 | 0.221 |
CLV_PCSK_KEX2_1 | 476 | 478 | PF00082 | 0.265 |
CLV_PCSK_KEX2_1 | 528 | 530 | PF00082 | 0.211 |
CLV_PCSK_KEX2_1 | 75 | 77 | PF00082 | 0.237 |
CLV_PCSK_PC1ET2_1 | 124 | 126 | PF00082 | 0.263 |
CLV_PCSK_PC1ET2_1 | 476 | 478 | PF00082 | 0.265 |
CLV_PCSK_PC1ET2_1 | 528 | 530 | PF00082 | 0.211 |
CLV_PCSK_PC1ET2_1 | 75 | 77 | PF00082 | 0.181 |
CLV_PCSK_SKI1_1 | 193 | 197 | PF00082 | 0.263 |
CLV_PCSK_SKI1_1 | 44 | 48 | PF00082 | 0.267 |
CLV_PCSK_SKI1_1 | 597 | 601 | PF00082 | 0.255 |
CLV_PCSK_SKI1_1 | 645 | 649 | PF00082 | 0.314 |
DEG_SCF_FBW7_1 | 458 | 463 | PF00400 | 0.256 |
DOC_MAPK_gen_1 | 221 | 228 | PF00069 | 0.486 |
DOC_MAPK_gen_1 | 417 | 425 | PF00069 | 0.421 |
DOC_MAPK_gen_1 | 643 | 651 | PF00069 | 0.254 |
DOC_MAPK_HePTP_8 | 497 | 509 | PF00069 | 0.467 |
DOC_MAPK_MEF2A_6 | 318 | 327 | PF00069 | 0.421 |
DOC_MAPK_MEF2A_6 | 500 | 509 | PF00069 | 0.573 |
DOC_MAPK_MEF2A_6 | 535 | 543 | PF00069 | 0.421 |
DOC_MAPK_MEF2A_6 | 643 | 651 | PF00069 | 0.254 |
DOC_PP2B_LxvP_1 | 226 | 229 | PF13499 | 0.463 |
DOC_PP2B_PxIxI_1 | 538 | 544 | PF00149 | 0.463 |
DOC_PP4_FxxP_1 | 106 | 109 | PF00568 | 0.421 |
DOC_USP7_MATH_1 | 195 | 199 | PF00917 | 0.436 |
DOC_USP7_MATH_1 | 521 | 525 | PF00917 | 0.458 |
DOC_USP7_UBL2_3 | 120 | 124 | PF12436 | 0.421 |
DOC_USP7_UBL2_3 | 189 | 193 | PF12436 | 0.441 |
DOC_USP7_UBL2_3 | 631 | 635 | PF12436 | 0.306 |
DOC_WW_Pin1_4 | 456 | 461 | PF00397 | 0.279 |
DOC_WW_Pin1_4 | 598 | 603 | PF00397 | 0.255 |
LIG_14-3-3_CanoR_1 | 125 | 135 | PF00244 | 0.436 |
LIG_14-3-3_CanoR_1 | 20 | 30 | PF00244 | 0.421 |
LIG_14-3-3_CanoR_1 | 221 | 227 | PF00244 | 0.468 |
LIG_14-3-3_CanoR_1 | 358 | 362 | PF00244 | 0.463 |
LIG_14-3-3_CanoR_1 | 535 | 539 | PF00244 | 0.350 |
LIG_Actin_WH2_2 | 135 | 152 | PF00022 | 0.463 |
LIG_Actin_WH2_2 | 303 | 320 | PF00022 | 0.463 |
LIG_Actin_WH2_2 | 412 | 429 | PF00022 | 0.421 |
LIG_APCC_ABBA_1 | 359 | 364 | PF00400 | 0.463 |
LIG_APCC_ABBA_1 | 382 | 387 | PF00400 | 0.421 |
LIG_APCC_ABBAyCdc20_2 | 358 | 364 | PF00400 | 0.463 |
LIG_BRCT_BRCA1_1 | 523 | 527 | PF00533 | 0.436 |
LIG_Clathr_ClatBox_1 | 624 | 628 | PF01394 | 0.235 |
LIG_Clathr_ClatBox_1 | 661 | 665 | PF01394 | 0.320 |
LIG_FHA_1 | 223 | 229 | PF00498 | 0.468 |
LIG_FHA_1 | 30 | 36 | PF00498 | 0.421 |
LIG_FHA_1 | 302 | 308 | PF00498 | 0.445 |
LIG_FHA_1 | 399 | 405 | PF00498 | 0.441 |
LIG_FHA_1 | 440 | 446 | PF00498 | 0.427 |
LIG_FHA_1 | 478 | 484 | PF00498 | 0.476 |
LIG_FHA_1 | 555 | 561 | PF00498 | 0.460 |
LIG_FHA_1 | 568 | 574 | PF00498 | 0.346 |
LIG_FHA_1 | 594 | 600 | PF00498 | 0.298 |
LIG_FHA_2 | 142 | 148 | PF00498 | 0.467 |
LIG_FHA_2 | 306 | 312 | PF00498 | 0.421 |
LIG_FHA_2 | 326 | 332 | PF00498 | 0.420 |
LIG_FHA_2 | 36 | 42 | PF00498 | 0.421 |
LIG_FHA_2 | 457 | 463 | PF00498 | 0.495 |
LIG_FHA_2 | 652 | 658 | PF00498 | 0.264 |
LIG_LIR_Apic_2 | 360 | 365 | PF02991 | 0.421 |
LIG_LIR_Apic_2 | 383 | 388 | PF02991 | 0.421 |
LIG_LIR_Gen_1 | 62 | 71 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 383 | 389 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 524 | 530 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 537 | 541 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 62 | 67 | PF02991 | 0.421 |
LIG_LYPXL_yS_3 | 157 | 160 | PF13949 | 0.421 |
LIG_LYPXL_yS_3 | 538 | 541 | PF13949 | 0.467 |
LIG_Pex14_1 | 534 | 538 | PF04695 | 0.421 |
LIG_SH2_CRK | 386 | 390 | PF00017 | 0.421 |
LIG_SH2_CRK | 86 | 90 | PF00017 | 0.421 |
LIG_SH2_NCK_1 | 36 | 40 | PF00017 | 0.463 |
LIG_SH2_NCK_1 | 467 | 471 | PF00017 | 0.302 |
LIG_SH2_PTP2 | 494 | 497 | PF00017 | 0.463 |
LIG_SH2_SRC | 362 | 365 | PF00017 | 0.421 |
LIG_SH2_STAP1 | 467 | 471 | PF00017 | 0.316 |
LIG_SH2_STAT3 | 508 | 511 | PF00017 | 0.467 |
LIG_SH2_STAT3 | 562 | 565 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 227 | 230 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 272 | 275 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 289 | 292 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 352 | 355 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 414 | 417 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 444 | 447 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 482 | 485 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 494 | 497 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 508 | 511 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 64 | 67 | PF00017 | 0.455 |
LIG_SH3_1 | 362 | 368 | PF00018 | 0.463 |
LIG_SH3_3 | 152 | 158 | PF00018 | 0.463 |
LIG_SH3_3 | 278 | 284 | PF00018 | 0.417 |
LIG_SH3_3 | 296 | 302 | PF00018 | 0.421 |
LIG_SH3_3 | 362 | 368 | PF00018 | 0.463 |
LIG_SH3_3 | 427 | 433 | PF00018 | 0.420 |
LIG_SH3_3 | 533 | 539 | PF00018 | 0.486 |
LIG_SH3_3 | 596 | 602 | PF00018 | 0.208 |
LIG_SUMO_SIM_anti_2 | 308 | 314 | PF11976 | 0.421 |
LIG_SUMO_SIM_par_1 | 31 | 38 | PF11976 | 0.421 |
LIG_SUMO_SIM_par_1 | 322 | 328 | PF11976 | 0.422 |
LIG_SUMO_SIM_par_1 | 622 | 628 | PF11976 | 0.314 |
LIG_SUMO_SIM_par_1 | 656 | 665 | PF11976 | 0.313 |
LIG_TRAF2_1 | 459 | 462 | PF00917 | 0.385 |
LIG_TRAF2_1 | 499 | 502 | PF00917 | 0.467 |
LIG_TRAF2_1 | 620 | 623 | PF00917 | 0.314 |
LIG_TYR_ITIM | 384 | 389 | PF00017 | 0.421 |
LIG_TYR_ITIM | 536 | 541 | PF00017 | 0.467 |
LIG_UBA3_1 | 389 | 398 | PF00899 | 0.463 |
LIG_UBA3_1 | 624 | 631 | PF00899 | 0.255 |
MOD_CK1_1 | 274 | 280 | PF00069 | 0.493 |
MOD_CK1_1 | 380 | 386 | PF00069 | 0.427 |
MOD_CK1_1 | 60 | 66 | PF00069 | 0.421 |
MOD_CK2_1 | 35 | 41 | PF00069 | 0.421 |
MOD_CK2_1 | 456 | 462 | PF00069 | 0.445 |
MOD_CK2_1 | 512 | 518 | PF00069 | 0.463 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.238 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.242 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.290 |
MOD_GlcNHglycan | 373 | 376 | PF01048 | 0.268 |
MOD_GlcNHglycan | 436 | 439 | PF01048 | 0.263 |
MOD_GlcNHglycan | 523 | 526 | PF01048 | 0.239 |
MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.210 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.436 |
MOD_GSK3_1 | 301 | 308 | PF00069 | 0.421 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.463 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.557 |
MOD_GSK3_1 | 554 | 561 | PF00069 | 0.446 |
MOD_GSK3_1 | 574 | 581 | PF00069 | 0.432 |
MOD_GSK3_1 | 589 | 596 | PF00069 | 0.491 |
MOD_GSK3_1 | 651 | 658 | PF00069 | 0.284 |
MOD_N-GLC_1 | 176 | 181 | PF02516 | 0.210 |
MOD_N-GLC_2 | 422 | 424 | PF02516 | 0.221 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.436 |
MOD_NEK2_1 | 493 | 498 | PF00069 | 0.443 |
MOD_NEK2_1 | 512 | 517 | PF00069 | 0.515 |
MOD_NEK2_1 | 566 | 571 | PF00069 | 0.421 |
MOD_NEK2_2 | 357 | 362 | PF00069 | 0.463 |
MOD_OFUCOSY | 19 | 25 | PF10250 | 0.221 |
MOD_PIKK_1 | 176 | 182 | PF00454 | 0.389 |
MOD_PIKK_1 | 325 | 331 | PF00454 | 0.487 |
MOD_PIKK_1 | 377 | 383 | PF00454 | 0.421 |
MOD_PIKK_1 | 460 | 466 | PF00454 | 0.420 |
MOD_PK_1 | 231 | 237 | PF00069 | 0.421 |
MOD_PKA_2 | 357 | 363 | PF00069 | 0.421 |
MOD_PKA_2 | 534 | 540 | PF00069 | 0.424 |
MOD_PKA_2 | 547 | 553 | PF00069 | 0.407 |
MOD_Plk_1 | 231 | 237 | PF00069 | 0.421 |
MOD_Plk_1 | 460 | 466 | PF00069 | 0.369 |
MOD_Plk_1 | 477 | 483 | PF00069 | 0.380 |
MOD_Plk_1 | 512 | 518 | PF00069 | 0.467 |
MOD_Plk_1 | 558 | 564 | PF00069 | 0.446 |
MOD_Plk_2-3 | 110 | 116 | PF00069 | 0.463 |
MOD_Plk_2-3 | 623 | 629 | PF00069 | 0.255 |
MOD_Plk_4 | 222 | 228 | PF00069 | 0.463 |
MOD_Plk_4 | 245 | 251 | PF00069 | 0.490 |
MOD_Plk_4 | 357 | 363 | PF00069 | 0.483 |
MOD_Plk_4 | 547 | 553 | PF00069 | 0.421 |
MOD_Plk_4 | 578 | 584 | PF00069 | 0.442 |
MOD_Plk_4 | 60 | 66 | PF00069 | 0.421 |
MOD_Plk_4 | 614 | 620 | PF00069 | 0.291 |
MOD_ProDKin_1 | 456 | 462 | PF00069 | 0.270 |
MOD_ProDKin_1 | 598 | 604 | PF00069 | 0.255 |
MOD_SUMO_for_1 | 475 | 478 | PF00179 | 0.467 |
MOD_SUMO_rev_2 | 119 | 126 | PF00179 | 0.463 |
MOD_SUMO_rev_2 | 186 | 195 | PF00179 | 0.463 |
MOD_SUMO_rev_2 | 248 | 255 | PF00179 | 0.421 |
MOD_SUMO_rev_2 | 326 | 334 | PF00179 | 0.410 |
MOD_SUMO_rev_2 | 641 | 649 | PF00179 | 0.261 |
TRG_DiLeu_BaEn_1 | 461 | 466 | PF01217 | 0.372 |
TRG_DiLeu_BaEn_4 | 622 | 628 | PF01217 | 0.314 |
TRG_DiLeu_BaLyEn_6 | 385 | 390 | PF01217 | 0.421 |
TRG_DiLeu_BaLyEn_6 | 536 | 541 | PF01217 | 0.350 |
TRG_ENDOCYTIC_2 | 157 | 160 | PF00928 | 0.421 |
TRG_ENDOCYTIC_2 | 184 | 187 | PF00928 | 0.467 |
TRG_ENDOCYTIC_2 | 386 | 389 | PF00928 | 0.421 |
TRG_ENDOCYTIC_2 | 494 | 497 | PF00928 | 0.463 |
TRG_ENDOCYTIC_2 | 538 | 541 | PF00928 | 0.467 |
TRG_ENDOCYTIC_2 | 64 | 67 | PF00928 | 0.421 |
TRG_ENDOCYTIC_2 | 86 | 89 | PF00928 | 0.421 |
TRG_NES_CRM1_1 | 578 | 591 | PF08389 | 0.428 |
TRG_Pf-PMV_PEXEL_1 | 200 | 204 | PF00026 | 0.221 |
TRG_Pf-PMV_PEXEL_1 | 409 | 413 | PF00026 | 0.292 |
TRG_Pf-PMV_PEXEL_1 | 510 | 514 | PF00026 | 0.241 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P730 | Leptomonas seymouri | 84% | 100% |
A0A0N1HV47 | Leptomonas seymouri | 38% | 97% |
A0A0S4IX46 | Bodo saltans | 39% | 98% |
A0A0S4JIQ8 | Bodo saltans | 66% | 100% |
A0A1X0NJV2 | Trypanosomatidae | 37% | 98% |
A0A3Q8IKH3 | Leishmania donovani | 38% | 97% |
A0A422NEZ1 | Trypanosoma rangeli | 38% | 98% |
A0A451EJ63 | Leishmania donovani | 96% | 100% |
A4H339 | Leishmania braziliensis | 92% | 100% |
A4HJV8 | Leishmania braziliensis | 37% | 100% |
A4HRC6 | Leishmania infantum | 96% | 100% |
A4I7C0 | Leishmania infantum | 38% | 97% |
C9ZWI5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 90% |
D3DJ42 | Hydrogenobacter thermophilus (strain DSM 6534 / IAM 12695 / TK-6) | 45% | 100% |
E9ABZ4 | Leishmania major | 96% | 100% |
E9B2B3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 97% |
I3R7G3 | Haloferax mediterranei (strain ATCC 33500 / DSM 1411 / JCM 8866 / NBRC 14739 / NCIMB 2177 / R-4) | 38% | 100% |
O30019 | Archaeoglobus fulgidus (strain ATCC 49558 / DSM 4304 / JCM 9628 / NBRC 100126 / VC-16) | 46% | 100% |
O34544 | Bacillus subtilis (strain 168) | 48% | 100% |
P05165 | Homo sapiens | 52% | 91% |
P0A509 | Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) | 50% | 100% |
P0DTA4 | Sus scrofa | 52% | 91% |
P14882 | Rattus norvegicus | 51% | 90% |
P43873 | Haemophilus influenzae (strain ATCC 51907 / DSM 11121 / KW20 / Rd) | 49% | 100% |
P9WPQ2 | Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) | 50% | 100% |
P9WPQ3 | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) | 50% | 100% |
Q19842 | Caenorhabditis elegans | 50% | 92% |
Q2QMG2 | Oryza sativa subsp. japonica | 47% | 90% |
Q42523 | Arabidopsis thaliana | 37% | 91% |
Q4Q5U3 | Leishmania major | 38% | 100% |
Q58626 | Methanocaldococcus jannaschii (strain ATCC 43067 / DSM 2661 / JAL-1 / JCM 10045 / NBRC 100440) | 49% | 100% |
Q5I0C3 | Rattus norvegicus | 37% | 93% |
Q5LUF3 | Ruegeria pomeroyi (strain ATCC 700808 / DSM 15171 / DSS-3) | 47% | 98% |
Q612F5 | Caenorhabditis briggsae | 50% | 90% |
Q91ZA3 | Mus musculus | 51% | 92% |
Q96RQ3 | Homo sapiens | 39% | 92% |
Q99MR8 | Mus musculus | 37% | 93% |
V5BDW2 | Trypanosoma cruzi | 37% | 95% |