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: 1 |
NetGPI | no | yes: 0, no: 1 |
Related structures:
AlphaFold database: A4H8A1
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 2 |
GO:0003676 | nucleic acid binding | 3 | 2 |
GO:0003824 | catalytic activity | 1 | 2 |
GO:0004386 | helicase activity | 2 | 2 |
GO:0005488 | binding | 1 | 2 |
GO:0005524 | ATP binding | 5 | 2 |
GO:0016787 | hydrolase activity | 2 | 2 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 2 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 2 |
GO:0017076 | purine nucleotide binding | 4 | 2 |
GO:0030554 | adenyl nucleotide binding | 5 | 2 |
GO:0032553 | ribonucleotide binding | 3 | 2 |
GO:0032555 | purine ribonucleotide binding | 4 | 2 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 2 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 2 |
GO:0036094 | small molecule binding | 2 | 2 |
GO:0043167 | ion binding | 2 | 2 |
GO:0043168 | anion binding | 3 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 2 |
GO:0097367 | carbohydrate derivative binding | 2 | 2 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 2 |
GO:0140657 | ATP-dependent activity | 1 | 2 |
GO:1901265 | nucleoside phosphate binding | 3 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 171 | 175 | PF00656 | 0.825 |
CLV_C14_Caspase3-7 | 37 | 41 | PF00656 | 0.833 |
CLV_C14_Caspase3-7 | 526 | 530 | PF00656 | 0.625 |
CLV_MEL_PAP_1 | 600 | 606 | PF00089 | 0.425 |
CLV_NRD_NRD_1 | 407 | 409 | PF00675 | 0.425 |
CLV_NRD_NRD_1 | 470 | 472 | PF00675 | 0.425 |
CLV_NRD_NRD_1 | 532 | 534 | PF00675 | 0.425 |
CLV_NRD_NRD_1 | 602 | 604 | PF00675 | 0.425 |
CLV_NRD_NRD_1 | 72 | 74 | PF00675 | 0.834 |
CLV_PCSK_FUR_1 | 70 | 74 | PF00082 | 0.827 |
CLV_PCSK_KEX2_1 | 255 | 257 | PF00082 | 0.815 |
CLV_PCSK_KEX2_1 | 395 | 397 | PF00082 | 0.425 |
CLV_PCSK_KEX2_1 | 407 | 409 | PF00082 | 0.275 |
CLV_PCSK_KEX2_1 | 470 | 472 | PF00082 | 0.425 |
CLV_PCSK_KEX2_1 | 50 | 52 | PF00082 | 0.840 |
CLV_PCSK_KEX2_1 | 532 | 534 | PF00082 | 0.425 |
CLV_PCSK_KEX2_1 | 601 | 603 | PF00082 | 0.425 |
CLV_PCSK_KEX2_1 | 72 | 74 | PF00082 | 0.834 |
CLV_PCSK_PC1ET2_1 | 255 | 257 | PF00082 | 0.815 |
CLV_PCSK_PC1ET2_1 | 395 | 397 | PF00082 | 0.425 |
CLV_PCSK_PC1ET2_1 | 50 | 52 | PF00082 | 0.840 |
CLV_PCSK_PC7_1 | 597 | 603 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 395 | 399 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 471 | 475 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 523 | 527 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 626 | 630 | PF00082 | 0.610 |
CLV_Separin_Metazoa | 424 | 428 | PF03568 | 0.625 |
DEG_APCC_DBOX_1 | 95 | 103 | PF00400 | 0.770 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.796 |
DEG_SCF_FBW7_1 | 156 | 163 | PF00400 | 0.730 |
DEG_SPOP_SBC_1 | 160 | 164 | PF00917 | 0.773 |
DEG_SPOP_SBC_1 | 288 | 292 | PF00917 | 0.636 |
DOC_CKS1_1 | 157 | 162 | PF01111 | 0.724 |
DOC_MAPK_gen_1 | 138 | 148 | PF00069 | 0.689 |
DOC_MAPK_gen_1 | 470 | 476 | PF00069 | 0.625 |
DOC_MAPK_gen_1 | 70 | 77 | PF00069 | 0.832 |
DOC_MAPK_MEF2A_6 | 495 | 502 | PF00069 | 0.625 |
DOC_PP1_RVXF_1 | 153 | 159 | PF00149 | 0.671 |
DOC_PP1_RVXF_1 | 71 | 78 | PF00149 | 0.834 |
DOC_PP2B_LxvP_1 | 221 | 224 | PF13499 | 0.703 |
DOC_PP2B_LxvP_1 | 500 | 503 | PF13499 | 0.625 |
DOC_PP2B_PxIxI_1 | 609 | 615 | PF00149 | 0.680 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.773 |
DOC_USP7_MATH_1 | 289 | 293 | PF00917 | 0.629 |
DOC_USP7_MATH_1 | 454 | 458 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 552 | 556 | PF00917 | 0.625 |
DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.711 |
DOC_WW_Pin1_4 | 162 | 167 | PF00397 | 0.706 |
DOC_WW_Pin1_4 | 336 | 341 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 548 | 553 | PF00397 | 0.625 |
DOC_WW_Pin1_4 | 90 | 95 | PF00397 | 0.840 |
LIG_14-3-3_CanoR_1 | 42 | 46 | PF00244 | 0.837 |
LIG_14-3-3_CanoR_1 | 482 | 489 | PF00244 | 0.625 |
LIG_14-3-3_CanoR_1 | 593 | 600 | PF00244 | 0.625 |
LIG_14-3-3_CanoR_1 | 601 | 610 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 613 | 619 | PF00244 | 0.249 |
LIG_Actin_WH2_2 | 95 | 110 | PF00022 | 0.751 |
LIG_BIR_III_2 | 442 | 446 | PF00653 | 0.625 |
LIG_BRCT_BRCA1_1 | 549 | 553 | PF00533 | 0.625 |
LIG_CSL_BTD_1 | 157 | 160 | PF09270 | 0.710 |
LIG_eIF4E_1 | 191 | 197 | PF01652 | 0.639 |
LIG_eIF4E_1 | 584 | 590 | PF01652 | 0.625 |
LIG_FAT_LD_1 | 139 | 147 | PF03623 | 0.686 |
LIG_FHA_1 | 152 | 158 | PF00498 | 0.666 |
LIG_FHA_1 | 178 | 184 | PF00498 | 0.684 |
LIG_FHA_1 | 325 | 331 | PF00498 | 0.808 |
LIG_FHA_1 | 332 | 338 | PF00498 | 0.632 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.837 |
LIG_FHA_1 | 519 | 525 | PF00498 | 0.625 |
LIG_FHA_1 | 584 | 590 | PF00498 | 0.625 |
LIG_FHA_2 | 321 | 327 | PF00498 | 0.806 |
LIG_FHA_2 | 368 | 374 | PF00498 | 0.625 |
LIG_FHA_2 | 506 | 512 | PF00498 | 0.625 |
LIG_FHA_2 | 524 | 530 | PF00498 | 0.400 |
LIG_FHA_2 | 552 | 558 | PF00498 | 0.625 |
LIG_FHA_2 | 85 | 91 | PF00498 | 0.857 |
LIG_GBD_Chelix_1 | 99 | 107 | PF00786 | 0.741 |
LIG_LIR_Apic_2 | 605 | 610 | PF02991 | 0.625 |
LIG_LIR_Gen_1 | 278 | 287 | PF02991 | 0.696 |
LIG_LIR_Gen_1 | 370 | 380 | PF02991 | 0.625 |
LIG_LIR_Gen_1 | 385 | 394 | PF02991 | 0.438 |
LIG_LIR_Gen_1 | 583 | 592 | PF02991 | 0.625 |
LIG_LIR_Nem_3 | 190 | 196 | PF02991 | 0.645 |
LIG_LIR_Nem_3 | 278 | 282 | PF02991 | 0.686 |
LIG_LIR_Nem_3 | 370 | 375 | PF02991 | 0.625 |
LIG_LIR_Nem_3 | 385 | 391 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 557 | 562 | PF02991 | 0.625 |
LIG_LIR_Nem_3 | 583 | 587 | PF02991 | 0.625 |
LIG_MYND_1 | 445 | 449 | PF01753 | 0.625 |
LIG_Pex14_2 | 618 | 622 | PF04695 | 0.580 |
LIG_REV1ctd_RIR_1 | 626 | 633 | PF16727 | 0.629 |
LIG_SH2_CRK | 388 | 392 | PF00017 | 0.625 |
LIG_SH2_CRK | 504 | 508 | PF00017 | 0.625 |
LIG_SH2_CRK | 584 | 588 | PF00017 | 0.625 |
LIG_SH2_GRB2like | 504 | 507 | PF00017 | 0.625 |
LIG_SH2_NCK_1 | 388 | 392 | PF00017 | 0.625 |
LIG_SH2_NCK_1 | 504 | 508 | PF00017 | 0.625 |
LIG_SH2_SRC | 504 | 507 | PF00017 | 0.625 |
LIG_SH2_STAP1 | 584 | 588 | PF00017 | 0.625 |
LIG_SH2_STAP1 | 9 | 13 | PF00017 | 0.774 |
LIG_SH2_STAT3 | 387 | 390 | PF00017 | 0.625 |
LIG_SH2_STAT5 | 147 | 150 | PF00017 | 0.695 |
LIG_SH2_STAT5 | 191 | 194 | PF00017 | 0.643 |
LIG_SH2_STAT5 | 562 | 565 | PF00017 | 0.625 |
LIG_SH2_STAT5 | 594 | 597 | PF00017 | 0.625 |
LIG_SH3_2 | 465 | 470 | PF14604 | 0.625 |
LIG_SH3_3 | 216 | 222 | PF00018 | 0.668 |
LIG_SH3_3 | 334 | 340 | PF00018 | 0.713 |
LIG_SH3_3 | 356 | 362 | PF00018 | 0.625 |
LIG_SH3_3 | 462 | 468 | PF00018 | 0.625 |
LIG_SH3_3 | 75 | 81 | PF00018 | 0.837 |
LIG_SH3_3 | 89 | 95 | PF00018 | 0.595 |
LIG_SUMO_SIM_anti_2 | 376 | 385 | PF11976 | 0.625 |
LIG_SUMO_SIM_anti_2 | 586 | 591 | PF11976 | 0.625 |
LIG_SUMO_SIM_par_1 | 376 | 385 | PF11976 | 0.625 |
LIG_SUMO_SIM_par_1 | 585 | 591 | PF11976 | 0.625 |
LIG_TRAF2_1 | 17 | 20 | PF00917 | 0.797 |
LIG_TRAF2_1 | 555 | 558 | PF00917 | 0.625 |
LIG_UBA3_1 | 103 | 108 | PF00899 | 0.727 |
LIG_WRC_WIRS_1 | 276 | 281 | PF05994 | 0.690 |
LIG_WW_3 | 93 | 97 | PF00397 | 0.809 |
MOD_CDC14_SPxK_1 | 93 | 96 | PF00782 | 0.824 |
MOD_CDK_SPxK_1 | 90 | 96 | PF00069 | 0.838 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.662 |
MOD_CK1_1 | 161 | 167 | PF00069 | 0.591 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.841 |
MOD_CK1_1 | 329 | 335 | PF00069 | 0.799 |
MOD_CK1_1 | 457 | 463 | PF00069 | 0.625 |
MOD_CK1_1 | 538 | 544 | PF00069 | 0.625 |
MOD_CK1_1 | 546 | 552 | PF00069 | 0.525 |
MOD_CK1_1 | 560 | 566 | PF00069 | 0.450 |
MOD_CK2_1 | 14 | 20 | PF00069 | 0.790 |
MOD_CK2_1 | 409 | 415 | PF00069 | 0.625 |
MOD_CK2_1 | 505 | 511 | PF00069 | 0.625 |
MOD_CK2_1 | 551 | 557 | PF00069 | 0.625 |
MOD_CK2_1 | 84 | 90 | PF00069 | 0.857 |
MOD_Cter_Amidation | 405 | 408 | PF01082 | 0.425 |
MOD_DYRK1A_RPxSP_1 | 336 | 340 | PF00069 | 0.683 |
MOD_GlcNHglycan | 227 | 230 | PF01048 | 0.827 |
MOD_GlcNHglycan | 242 | 246 | PF01048 | 0.550 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.747 |
MOD_GlcNHglycan | 302 | 305 | PF01048 | 0.631 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.841 |
MOD_GlcNHglycan | 411 | 414 | PF01048 | 0.425 |
MOD_GlcNHglycan | 417 | 420 | PF01048 | 0.350 |
MOD_GlcNHglycan | 433 | 436 | PF01048 | 0.225 |
MOD_GlcNHglycan | 454 | 457 | PF01048 | 0.425 |
MOD_GlcNHglycan | 537 | 540 | PF01048 | 0.425 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.521 |
MOD_GlcNHglycan | 542 | 545 | PF01048 | 0.363 |
MOD_GlcNHglycan | 554 | 557 | PF01048 | 0.213 |
MOD_GlcNHglycan | 604 | 607 | PF01048 | 0.425 |
MOD_GlcNHglycan | 622 | 625 | PF01048 | 0.254 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.683 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.555 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.857 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.736 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.804 |
MOD_GSK3_1 | 448 | 455 | PF00069 | 0.625 |
MOD_GSK3_1 | 519 | 526 | PF00069 | 0.625 |
MOD_GSK3_1 | 538 | 545 | PF00069 | 0.388 |
MOD_GSK3_1 | 547 | 554 | PF00069 | 0.513 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.830 |
MOD_N-GLC_1 | 225 | 230 | PF02516 | 0.817 |
MOD_N-GLC_1 | 82 | 87 | PF02516 | 0.853 |
MOD_N-GLC_2 | 571 | 573 | PF02516 | 0.425 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.670 |
MOD_NEK2_1 | 307 | 312 | PF00069 | 0.631 |
MOD_NEK2_1 | 382 | 387 | PF00069 | 0.625 |
MOD_NEK2_1 | 398 | 403 | PF00069 | 0.425 |
MOD_NEK2_1 | 535 | 540 | PF00069 | 0.625 |
MOD_NEK2_1 | 547 | 552 | PF00069 | 0.475 |
MOD_NEK2_1 | 566 | 571 | PF00069 | 0.388 |
MOD_PIKK_1 | 166 | 172 | PF00454 | 0.834 |
MOD_PIKK_1 | 307 | 313 | PF00454 | 0.634 |
MOD_PKA_1 | 407 | 413 | PF00069 | 0.625 |
MOD_PKA_1 | 602 | 608 | PF00069 | 0.625 |
MOD_PKA_2 | 31 | 37 | PF00069 | 0.854 |
MOD_PKA_2 | 407 | 413 | PF00069 | 0.625 |
MOD_PKA_2 | 41 | 47 | PF00069 | 0.661 |
MOD_PKA_2 | 481 | 487 | PF00069 | 0.625 |
MOD_PKA_2 | 52 | 58 | PF00069 | 0.647 |
MOD_PKA_2 | 592 | 598 | PF00069 | 0.625 |
MOD_PKA_2 | 602 | 608 | PF00069 | 0.500 |
MOD_Plk_1 | 241 | 247 | PF00069 | 0.815 |
MOD_Plk_1 | 262 | 268 | PF00069 | 0.788 |
MOD_Plk_1 | 557 | 563 | PF00069 | 0.625 |
MOD_Plk_2-3 | 14 | 20 | PF00069 | 0.790 |
MOD_Plk_4 | 349 | 355 | PF00069 | 0.557 |
MOD_Plk_4 | 374 | 380 | PF00069 | 0.625 |
MOD_Plk_4 | 583 | 589 | PF00069 | 0.625 |
MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.718 |
MOD_ProDKin_1 | 336 | 342 | PF00069 | 0.664 |
MOD_ProDKin_1 | 548 | 554 | PF00069 | 0.625 |
MOD_ProDKin_1 | 90 | 96 | PF00069 | 0.838 |
MOD_SUMO_rev_2 | 14 | 24 | PF00179 | 0.804 |
TRG_DiLeu_BaLyEn_6 | 138 | 143 | PF01217 | 0.680 |
TRG_DiLeu_BaLyEn_6 | 216 | 221 | PF01217 | 0.664 |
TRG_ENDOCYTIC_2 | 372 | 375 | PF00928 | 0.625 |
TRG_ENDOCYTIC_2 | 388 | 391 | PF00928 | 0.425 |
TRG_ENDOCYTIC_2 | 584 | 587 | PF00928 | 0.625 |
TRG_ER_diArg_1 | 600 | 603 | PF00400 | 0.625 |
TRG_ER_diArg_1 | 70 | 73 | PF00400 | 0.828 |
TRG_Pf-PMV_PEXEL_1 | 129 | 134 | PF00026 | 0.700 |
TRG_Pf-PMV_PEXEL_1 | 344 | 348 | PF00026 | 0.580 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A1CJ34 | Aspergillus clavatus (strain ATCC 1007 / CBS 513.65 / DSM 816 / NCTC 3887 / NRRL 1 / QM 1276 / 107) | 24% | 87% |
A1D8E4 | Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / CBS 544.65 / FGSC A1164 / JCM 1740 / NRRL 181 / WB 181) | 25% | 74% |
A2QY22 | Aspergillus niger (strain CBS 513.88 / FGSC A1513) | 26% | 73% |
A5DUW8 | Lodderomyces elongisporus (strain ATCC 11503 / CBS 2605 / JCM 1781 / NBRC 1676 / NRRL YB-4239) | 24% | 71% |
A7ERG1 | Sclerotinia sclerotiorum (strain ATCC 18683 / 1980 / Ss-1) | 25% | 71% |
F1R345 | Danio rerio | 28% | 71% |
Q4WWE9 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 26% | 81% |
Q5AD67 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 24% | 76% |
Q6AXC6 | Mus musculus | 27% | 70% |
Q6CAX3 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 24% | 79% |
Q92771 | Homo sapiens | 26% | 67% |