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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005739 | mitochondrion | 5 | 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:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QFB3
Term | Name | Level | Count |
---|---|---|---|
GO:0006743 | ubiquinone metabolic process | 5 | 2 |
GO:0006744 | ubiquinone biosynthetic process | 6 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009058 | biosynthetic process | 2 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0042180 | cellular ketone metabolic process | 3 | 2 |
GO:0042181 | ketone biosynthetic process | 4 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044249 | cellular biosynthetic process | 3 | 2 |
GO:0044281 | small molecule metabolic process | 2 | 2 |
GO:0044283 | small molecule biosynthetic process | 3 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901576 | organic substance biosynthetic process | 3 | 2 |
GO:1901661 | quinone metabolic process | 4 | 2 |
GO:1901663 | quinone biosynthetic process | 5 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 10 |
GO:0004497 | monooxygenase activity | 3 | 10 |
GO:0016491 | oxidoreductase activity | 2 | 10 |
GO:0000166 | nucleotide binding | 3 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0036094 | small molecule binding | 2 | 1 |
GO:0043167 | ion binding | 2 | 1 |
GO:0043168 | anion binding | 3 | 1 |
GO:0050660 | flavin adenine dinucleotide binding | 4 | 1 |
GO:0071949 | FAD binding | 5 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901265 | nucleoside phosphate binding | 3 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 563 | 567 | PF00656 | 0.524 |
CLV_NRD_NRD_1 | 141 | 143 | PF00675 | 0.675 |
CLV_NRD_NRD_1 | 196 | 198 | PF00675 | 0.412 |
CLV_NRD_NRD_1 | 256 | 258 | PF00675 | 0.490 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.612 |
CLV_NRD_NRD_1 | 333 | 335 | PF00675 | 0.611 |
CLV_NRD_NRD_1 | 344 | 346 | PF00675 | 0.502 |
CLV_NRD_NRD_1 | 410 | 412 | PF00675 | 0.426 |
CLV_NRD_NRD_1 | 580 | 582 | PF00675 | 0.466 |
CLV_PCSK_KEX2_1 | 141 | 143 | PF00082 | 0.675 |
CLV_PCSK_KEX2_1 | 196 | 198 | PF00082 | 0.412 |
CLV_PCSK_KEX2_1 | 256 | 258 | PF00082 | 0.490 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.574 |
CLV_PCSK_KEX2_1 | 333 | 335 | PF00082 | 0.656 |
CLV_PCSK_KEX2_1 | 409 | 411 | PF00082 | 0.463 |
CLV_PCSK_KEX2_1 | 580 | 582 | PF00082 | 0.495 |
CLV_PCSK_PC7_1 | 137 | 143 | PF00082 | 0.673 |
CLV_PCSK_PC7_1 | 405 | 411 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 196 | 200 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 256 | 260 | PF00082 | 0.371 |
CLV_PCSK_SKI1_1 | 569 | 573 | PF00082 | 0.426 |
CLV_Separin_Metazoa | 462 | 466 | PF03568 | 0.523 |
DEG_APCC_DBOX_1 | 195 | 203 | PF00400 | 0.514 |
DEG_APCC_DBOX_1 | 464 | 472 | PF00400 | 0.533 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.589 |
DEG_SPOP_SBC_1 | 175 | 179 | PF00917 | 0.672 |
DEG_SPOP_SBC_1 | 472 | 476 | PF00917 | 0.629 |
DOC_CYCLIN_RxL_1 | 253 | 260 | PF00134 | 0.412 |
DOC_MAPK_gen_1 | 208 | 217 | PF00069 | 0.480 |
DOC_MAPK_gen_1 | 333 | 342 | PF00069 | 0.517 |
DOC_MAPK_HePTP_8 | 207 | 219 | PF00069 | 0.350 |
DOC_MAPK_MEF2A_6 | 182 | 189 | PF00069 | 0.508 |
DOC_MAPK_MEF2A_6 | 210 | 219 | PF00069 | 0.482 |
DOC_MAPK_MEF2A_6 | 581 | 590 | PF00069 | 0.450 |
DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.782 |
DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.713 |
DOC_USP7_MATH_1 | 228 | 232 | PF00917 | 0.470 |
DOC_USP7_MATH_1 | 294 | 298 | PF00917 | 0.469 |
DOC_USP7_MATH_1 | 305 | 309 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 336 | 340 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 414 | 418 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 472 | 476 | PF00917 | 0.563 |
DOC_USP7_UBL2_3 | 346 | 350 | PF12436 | 0.476 |
DOC_USP7_UBL2_3 | 639 | 643 | PF12436 | 0.509 |
DOC_WW_Pin1_4 | 120 | 125 | PF00397 | 0.769 |
DOC_WW_Pin1_4 | 176 | 181 | PF00397 | 0.660 |
DOC_WW_Pin1_4 | 475 | 480 | PF00397 | 0.665 |
DOC_WW_Pin1_4 | 55 | 60 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 582 | 587 | PF00397 | 0.529 |
DOC_WW_Pin1_4 | 90 | 95 | PF00397 | 0.516 |
LIG_14-3-3_CanoR_1 | 334 | 342 | PF00244 | 0.627 |
LIG_14-3-3_CanoR_1 | 409 | 416 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 604 | 610 | PF00244 | 0.617 |
LIG_14-3-3_CanoR_1 | 629 | 635 | PF00244 | 0.519 |
LIG_14-3-3_CterR_2 | 652 | 655 | PF00244 | 0.581 |
LIG_APCC_ABBA_1 | 272 | 277 | PF00400 | 0.535 |
LIG_BRCT_BRCA1_1 | 440 | 444 | PF00533 | 0.457 |
LIG_BRCT_BRCA1_1 | 546 | 550 | PF00533 | 0.431 |
LIG_BRCT_BRCA1_1 | 76 | 80 | PF00533 | 0.514 |
LIG_Clathr_ClatBox_1 | 374 | 378 | PF01394 | 0.414 |
LIG_EH_1 | 521 | 525 | PF12763 | 0.374 |
LIG_FHA_1 | 113 | 119 | PF00498 | 0.812 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.486 |
LIG_FHA_1 | 320 | 326 | PF00498 | 0.578 |
LIG_FHA_1 | 410 | 416 | PF00498 | 0.496 |
LIG_FHA_1 | 503 | 509 | PF00498 | 0.507 |
LIG_FHA_1 | 85 | 91 | PF00498 | 0.425 |
LIG_FHA_2 | 606 | 612 | PF00498 | 0.630 |
LIG_FHA_2 | 630 | 636 | PF00498 | 0.542 |
LIG_FHA_2 | 86 | 92 | PF00498 | 0.433 |
LIG_LIR_Apic_2 | 47 | 51 | PF02991 | 0.741 |
LIG_LIR_Gen_1 | 184 | 194 | PF02991 | 0.484 |
LIG_LIR_Gen_1 | 357 | 364 | PF02991 | 0.400 |
LIG_LIR_Gen_1 | 441 | 451 | PF02991 | 0.364 |
LIG_LIR_Gen_1 | 500 | 511 | PF02991 | 0.422 |
LIG_LIR_Gen_1 | 585 | 594 | PF02991 | 0.526 |
LIG_LIR_Nem_3 | 181 | 186 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 188 | 194 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 357 | 361 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 432 | 438 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 441 | 447 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 47 | 52 | PF02991 | 0.641 |
LIG_LIR_Nem_3 | 500 | 506 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 585 | 590 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 628 | 634 | PF02991 | 0.598 |
LIG_LYPXL_yS_3 | 494 | 497 | PF13949 | 0.449 |
LIG_NRBOX | 254 | 260 | PF00104 | 0.413 |
LIG_Pex14_1 | 347 | 351 | PF04695 | 0.458 |
LIG_Pex14_1 | 606 | 610 | PF04695 | 0.613 |
LIG_PTB_Apo_2 | 36 | 43 | PF02174 | 0.577 |
LIG_PTB_Phospho_1 | 36 | 42 | PF10480 | 0.579 |
LIG_SH2_CRK | 136 | 140 | PF00017 | 0.664 |
LIG_SH2_CRK | 191 | 195 | PF00017 | 0.460 |
LIG_SH2_CRK | 358 | 362 | PF00017 | 0.375 |
LIG_SH2_CRK | 503 | 507 | PF00017 | 0.522 |
LIG_SH2_CRK | 551 | 555 | PF00017 | 0.410 |
LIG_SH2_CRK | 6 | 10 | PF00017 | 0.696 |
LIG_SH2_GRB2like | 557 | 560 | PF00017 | 0.495 |
LIG_SH2_NCK_1 | 191 | 195 | PF00017 | 0.479 |
LIG_SH2_NCK_1 | 503 | 507 | PF00017 | 0.522 |
LIG_SH2_SRC | 276 | 279 | PF00017 | 0.499 |
LIG_SH2_SRC | 634 | 637 | PF00017 | 0.522 |
LIG_SH2_STAP1 | 276 | 280 | PF00017 | 0.482 |
LIG_SH2_STAP1 | 351 | 355 | PF00017 | 0.440 |
LIG_SH2_STAP1 | 358 | 362 | PF00017 | 0.347 |
LIG_SH2_STAP1 | 546 | 550 | PF00017 | 0.451 |
LIG_SH2_STAP1 | 618 | 622 | PF00017 | 0.486 |
LIG_SH2_STAT3 | 42 | 45 | PF00017 | 0.662 |
LIG_SH2_STAT3 | 421 | 424 | PF00017 | 0.544 |
LIG_SH2_STAT3 | 449 | 452 | PF00017 | 0.467 |
LIG_SH2_STAT3 | 498 | 501 | PF00017 | 0.523 |
LIG_SH2_STAT5 | 15 | 18 | PF00017 | 0.593 |
LIG_SH2_STAT5 | 33 | 36 | PF00017 | 0.597 |
LIG_SH2_STAT5 | 467 | 470 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 498 | 501 | PF00017 | 0.484 |
LIG_SH2_STAT5 | 631 | 634 | PF00017 | 0.522 |
LIG_SH3_3 | 121 | 127 | PF00018 | 0.782 |
LIG_SH3_3 | 288 | 294 | PF00018 | 0.423 |
LIG_SH3_3 | 445 | 451 | PF00018 | 0.396 |
LIG_SH3_3 | 503 | 509 | PF00018 | 0.460 |
LIG_SH3_3 | 597 | 603 | PF00018 | 0.518 |
LIG_SUMO_SIM_par_1 | 373 | 378 | PF11976 | 0.416 |
LIG_TRAF2_1 | 316 | 319 | PF00917 | 0.620 |
LIG_TYR_ITIM | 189 | 194 | PF00017 | 0.488 |
LIG_TYR_ITIM | 274 | 279 | PF00017 | 0.493 |
LIG_TYR_ITIM | 356 | 361 | PF00017 | 0.397 |
LIG_WRC_WIRS_1 | 168 | 173 | PF05994 | 0.570 |
LIG_WRC_WIRS_1 | 484 | 489 | PF05994 | 0.484 |
MOD_CDC14_SPxK_1 | 179 | 182 | PF00782 | 0.647 |
MOD_CDC14_SPxK_1 | 58 | 61 | PF00782 | 0.521 |
MOD_CDK_SPxK_1 | 176 | 182 | PF00069 | 0.681 |
MOD_CDK_SPxK_1 | 55 | 61 | PF00069 | 0.556 |
MOD_CDK_SPxxK_3 | 582 | 589 | PF00069 | 0.535 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.752 |
MOD_CK1_1 | 125 | 131 | PF00069 | 0.732 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.789 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.684 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.636 |
MOD_CK1_1 | 181 | 187 | PF00069 | 0.549 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.473 |
MOD_CK1_1 | 266 | 272 | PF00069 | 0.559 |
MOD_CK1_1 | 308 | 314 | PF00069 | 0.676 |
MOD_CK1_1 | 417 | 423 | PF00069 | 0.617 |
MOD_CK1_1 | 473 | 479 | PF00069 | 0.630 |
MOD_CK1_1 | 486 | 492 | PF00069 | 0.421 |
MOD_CK2_1 | 312 | 318 | PF00069 | 0.593 |
MOD_CK2_1 | 605 | 611 | PF00069 | 0.588 |
MOD_CK2_1 | 85 | 91 | PF00069 | 0.403 |
MOD_GlcNHglycan | 17 | 21 | PF01048 | 0.603 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.765 |
MOD_GlcNHglycan | 268 | 271 | PF01048 | 0.584 |
MOD_GlcNHglycan | 296 | 300 | PF01048 | 0.517 |
MOD_GlcNHglycan | 342 | 345 | PF01048 | 0.536 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.183 |
MOD_GlcNHglycan | 416 | 419 | PF01048 | 0.672 |
MOD_GlcNHglycan | 424 | 427 | PF01048 | 0.463 |
MOD_GlcNHglycan | 509 | 512 | PF01048 | 0.372 |
MOD_GlcNHglycan | 563 | 566 | PF01048 | 0.456 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.388 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.350 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.676 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.784 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.740 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.797 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.512 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.670 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.551 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.398 |
MOD_GSK3_1 | 410 | 417 | PF00069 | 0.388 |
MOD_GSK3_1 | 438 | 445 | PF00069 | 0.462 |
MOD_GSK3_1 | 470 | 477 | PF00069 | 0.524 |
MOD_GSK3_1 | 625 | 632 | PF00069 | 0.628 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.592 |
MOD_LATS_1 | 408 | 414 | PF00433 | 0.575 |
MOD_N-GLC_1 | 312 | 317 | PF02516 | 0.678 |
MOD_N-GLC_2 | 599 | 601 | PF02516 | 0.591 |
MOD_NEK2_1 | 340 | 345 | PF00069 | 0.491 |
MOD_NEK2_1 | 471 | 476 | PF00069 | 0.587 |
MOD_NEK2_1 | 502 | 507 | PF00069 | 0.447 |
MOD_NEK2_1 | 625 | 630 | PF00069 | 0.573 |
MOD_NEK2_1 | 74 | 79 | PF00069 | 0.493 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.593 |
MOD_NEK2_2 | 605 | 610 | PF00069 | 0.618 |
MOD_PKA_1 | 409 | 415 | PF00069 | 0.524 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.608 |
MOD_PKA_2 | 409 | 415 | PF00069 | 0.502 |
MOD_PKA_2 | 560 | 566 | PF00069 | 0.520 |
MOD_Plk_1 | 295 | 301 | PF00069 | 0.518 |
MOD_Plk_1 | 305 | 311 | PF00069 | 0.501 |
MOD_Plk_4 | 228 | 234 | PF00069 | 0.467 |
MOD_Plk_4 | 493 | 499 | PF00069 | 0.409 |
MOD_Plk_4 | 605 | 611 | PF00069 | 0.611 |
MOD_Plk_4 | 85 | 91 | PF00069 | 0.406 |
MOD_ProDKin_1 | 120 | 126 | PF00069 | 0.767 |
MOD_ProDKin_1 | 176 | 182 | PF00069 | 0.643 |
MOD_ProDKin_1 | 475 | 481 | PF00069 | 0.656 |
MOD_ProDKin_1 | 55 | 61 | PF00069 | 0.556 |
MOD_ProDKin_1 | 582 | 588 | PF00069 | 0.528 |
MOD_ProDKin_1 | 90 | 96 | PF00069 | 0.518 |
MOD_SUMO_for_1 | 99 | 102 | PF00179 | 0.583 |
MOD_SUMO_rev_2 | 343 | 352 | PF00179 | 0.576 |
TRG_DiLeu_BaEn_2 | 482 | 488 | PF01217 | 0.569 |
TRG_DiLeu_BaLyEn_6 | 254 | 259 | PF01217 | 0.446 |
TRG_DiLeu_BaLyEn_6 | 4 | 9 | PF01217 | 0.619 |
TRG_ENDOCYTIC_2 | 183 | 186 | PF00928 | 0.497 |
TRG_ENDOCYTIC_2 | 191 | 194 | PF00928 | 0.406 |
TRG_ENDOCYTIC_2 | 276 | 279 | PF00928 | 0.489 |
TRG_ENDOCYTIC_2 | 358 | 361 | PF00928 | 0.379 |
TRG_ENDOCYTIC_2 | 494 | 497 | PF00928 | 0.439 |
TRG_ENDOCYTIC_2 | 503 | 506 | PF00928 | 0.396 |
TRG_ENDOCYTIC_2 | 551 | 554 | PF00928 | 0.404 |
TRG_ENDOCYTIC_2 | 594 | 597 | PF00928 | 0.484 |
TRG_ENDOCYTIC_2 | 6 | 9 | PF00928 | 0.693 |
TRG_ER_diArg_1 | 140 | 142 | PF00400 | 0.664 |
TRG_ER_diArg_1 | 2 | 4 | PF00400 | 0.626 |
TRG_ER_diArg_1 | 207 | 210 | PF00400 | 0.353 |
TRG_ER_diArg_1 | 255 | 257 | PF00400 | 0.484 |
TRG_ER_diArg_1 | 332 | 334 | PF00400 | 0.675 |
TRG_ER_diArg_1 | 409 | 411 | PF00400 | 0.523 |
TRG_Pf-PMV_PEXEL_1 | 256 | 260 | PF00026 | 0.428 |
TRG_Pf-PMV_PEXEL_1 | 30 | 35 | PF00026 | 0.717 |
TRG_Pf-PMV_PEXEL_1 | 372 | 376 | PF00026 | 0.413 |
TRG_Pf-PMV_PEXEL_1 | 569 | 573 | PF00026 | 0.426 |
TRG_Pf-PMV_PEXEL_1 | 620 | 624 | PF00026 | 0.605 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HTW3 | Leptomonas seymouri | 73% | 100% |
A0A0S4JRA1 | Bodo saltans | 47% | 100% |
A0A1X0NTX5 | Trypanosomatidae | 56% | 100% |
A0A3S5H6U9 | Leishmania donovani | 96% | 100% |
A4HWG9 | Leishmania infantum | 96% | 100% |
C9ZXY4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 100% |
E9AQ70 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
V5DL32 | Trypanosoma cruzi | 54% | 100% |