Metal Binding, Uncharacterized
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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005730 | nucleolus | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4I5F4
Term | Name | Level | Count |
---|---|---|---|
GO:0006414 | translational elongation | 5 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009058 | biosynthetic process | 2 | 11 |
GO:0009059 | macromolecule biosynthetic process | 4 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0034645 | obsolete cellular macromolecule biosynthetic process | 4 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044249 | cellular biosynthetic process | 3 | 11 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0072344 | rescue of stalled ribosome | 6 | 11 |
GO:1901576 | organic substance biosynthetic process | 3 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0016567 | protein ubiquitination | 7 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0032446 | protein modification by small protein conjugation | 6 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004842 | ubiquitin-protein transferase activity | 4 | 11 |
GO:0016740 | transferase activity | 2 | 11 |
GO:0019787 | ubiquitin-like protein transferase activity | 3 | 11 |
GO:0061630 | ubiquitin protein ligase activity | 5 | 11 |
GO:0061659 | ubiquitin-like protein ligase activity | 4 | 11 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 11 |
GO:0005488 | binding | 1 | 4 |
GO:0043021 | ribonucleoprotein complex binding | 3 | 1 |
GO:0043022 | ribosome binding | 4 | 1 |
GO:0043167 | ion binding | 2 | 4 |
GO:0043169 | cation binding | 3 | 4 |
GO:0044877 | protein-containing complex binding | 2 | 1 |
GO:0046872 | metal ion binding | 4 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 103 | 105 | PF00675 | 0.575 |
CLV_NRD_NRD_1 | 360 | 362 | PF00675 | 0.649 |
CLV_NRD_NRD_1 | 546 | 548 | PF00675 | 0.570 |
CLV_NRD_NRD_1 | 590 | 592 | PF00675 | 0.690 |
CLV_NRD_NRD_1 | 705 | 707 | PF00675 | 0.645 |
CLV_NRD_NRD_1 | 73 | 75 | PF00675 | 0.410 |
CLV_PCSK_KEX2_1 | 103 | 105 | PF00082 | 0.575 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.543 |
CLV_PCSK_KEX2_1 | 360 | 362 | PF00082 | 0.647 |
CLV_PCSK_KEX2_1 | 705 | 707 | PF00082 | 0.643 |
CLV_PCSK_PC1ET2_1 | 213 | 215 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 104 | 108 | PF00082 | 0.508 |
CLV_PCSK_SKI1_1 | 173 | 177 | PF00082 | 0.334 |
CLV_PCSK_SKI1_1 | 460 | 464 | PF00082 | 0.431 |
CLV_PCSK_SKI1_1 | 592 | 596 | PF00082 | 0.640 |
CLV_PCSK_SKI1_1 | 597 | 601 | PF00082 | 0.617 |
CLV_PCSK_SKI1_1 | 75 | 79 | PF00082 | 0.355 |
DEG_APCC_KENBOX_2 | 351 | 355 | PF00400 | 0.636 |
DEG_SPOP_SBC_1 | 404 | 408 | PF00917 | 0.681 |
DEG_SPOP_SBC_1 | 422 | 426 | PF00917 | 0.524 |
DEG_SPOP_SBC_1 | 634 | 638 | PF00917 | 0.723 |
DOC_ANK_TNKS_1 | 704 | 711 | PF00023 | 0.538 |
DOC_CKS1_1 | 669 | 674 | PF01111 | 0.603 |
DOC_MAPK_gen_1 | 74 | 82 | PF00069 | 0.364 |
DOC_PP1_RVXF_1 | 297 | 303 | PF00149 | 0.503 |
DOC_PP4_FxxP_1 | 497 | 500 | PF00568 | 0.516 |
DOC_USP7_MATH_1 | 134 | 138 | PF00917 | 0.418 |
DOC_USP7_MATH_1 | 310 | 314 | PF00917 | 0.581 |
DOC_USP7_MATH_1 | 319 | 323 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 325 | 329 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 404 | 408 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 414 | 418 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 423 | 427 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 567 | 571 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 577 | 581 | PF00917 | 0.597 |
DOC_USP7_MATH_1 | 626 | 630 | PF00917 | 0.737 |
DOC_USP7_MATH_1 | 635 | 639 | PF00917 | 0.659 |
DOC_USP7_MATH_1 | 642 | 646 | PF00917 | 0.627 |
DOC_USP7_MATH_1 | 661 | 665 | PF00917 | 0.441 |
DOC_USP7_MATH_1 | 673 | 677 | PF00917 | 0.607 |
DOC_WW_Pin1_4 | 115 | 120 | PF00397 | 0.475 |
DOC_WW_Pin1_4 | 22 | 27 | PF00397 | 0.648 |
DOC_WW_Pin1_4 | 300 | 305 | PF00397 | 0.585 |
DOC_WW_Pin1_4 | 461 | 466 | PF00397 | 0.539 |
DOC_WW_Pin1_4 | 578 | 583 | PF00397 | 0.752 |
DOC_WW_Pin1_4 | 584 | 589 | PF00397 | 0.662 |
DOC_WW_Pin1_4 | 668 | 673 | PF00397 | 0.719 |
DOC_WW_Pin1_4 | 678 | 683 | PF00397 | 0.663 |
LIG_14-3-3_CanoR_1 | 103 | 112 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 200 | 204 | PF00244 | 0.556 |
LIG_14-3-3_CanoR_1 | 240 | 246 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 419 | 423 | PF00244 | 0.725 |
LIG_14-3-3_CanoR_1 | 61 | 66 | PF00244 | 0.410 |
LIG_Actin_WH2_2 | 98 | 115 | PF00022 | 0.462 |
LIG_AP2alpha_2 | 145 | 147 | PF02296 | 0.494 |
LIG_APCC_ABBA_1 | 24 | 29 | PF00400 | 0.518 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.713 |
LIG_BRCT_BRCA1_1 | 387 | 391 | PF00533 | 0.432 |
LIG_BRCT_BRCA1_1 | 424 | 428 | PF00533 | 0.681 |
LIG_BRCT_BRCA1_1 | 664 | 668 | PF00533 | 0.564 |
LIG_eIF4E_1 | 219 | 225 | PF01652 | 0.355 |
LIG_EVH1_2 | 207 | 211 | PF00568 | 0.425 |
LIG_FHA_1 | 130 | 136 | PF00498 | 0.448 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.410 |
LIG_FHA_1 | 318 | 324 | PF00498 | 0.560 |
LIG_FHA_1 | 393 | 399 | PF00498 | 0.570 |
LIG_FHA_1 | 511 | 517 | PF00498 | 0.408 |
LIG_FHA_1 | 533 | 539 | PF00498 | 0.588 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.407 |
LIG_LIR_Apic_2 | 130 | 134 | PF02991 | 0.332 |
LIG_LIR_Apic_2 | 495 | 500 | PF02991 | 0.513 |
LIG_LIR_Gen_1 | 145 | 153 | PF02991 | 0.436 |
LIG_LIR_Gen_1 | 162 | 170 | PF02991 | 0.341 |
LIG_LIR_Gen_1 | 336 | 343 | PF02991 | 0.431 |
LIG_LIR_Gen_1 | 467 | 474 | PF02991 | 0.548 |
LIG_LIR_Gen_1 | 486 | 497 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 162 | 168 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 244 | 248 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 336 | 340 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 388 | 394 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 467 | 471 | PF02991 | 0.536 |
LIG_LIR_Nem_3 | 485 | 491 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 505 | 510 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 693 | 699 | PF02991 | 0.594 |
LIG_LRP6_Inhibitor_1 | 699 | 705 | PF00058 | 0.604 |
LIG_NRP_CendR_1 | 722 | 723 | PF00754 | 0.729 |
LIG_PCNA_PIPBox_1 | 150 | 159 | PF02747 | 0.359 |
LIG_PCNA_yPIPBox_3 | 519 | 527 | PF02747 | 0.395 |
LIG_Pex14_1 | 139 | 143 | PF04695 | 0.418 |
LIG_Pex14_2 | 243 | 247 | PF04695 | 0.486 |
LIG_Pex14_2 | 337 | 341 | PF04695 | 0.528 |
LIG_Pex14_2 | 503 | 507 | PF04695 | 0.414 |
LIG_SH2_CRK | 131 | 135 | PF00017 | 0.362 |
LIG_SH2_CRK | 489 | 493 | PF00017 | 0.401 |
LIG_SH2_SRC | 143 | 146 | PF00017 | 0.494 |
LIG_SH2_STAP1 | 183 | 187 | PF00017 | 0.428 |
LIG_SH2_STAP1 | 233 | 237 | PF00017 | 0.483 |
LIG_SH2_STAP1 | 27 | 31 | PF00017 | 0.455 |
LIG_SH2_STAP1 | 474 | 478 | PF00017 | 0.484 |
LIG_SH2_STAP1 | 489 | 493 | PF00017 | 0.531 |
LIG_SH2_STAT5 | 131 | 134 | PF00017 | 0.298 |
LIG_SH2_STAT5 | 165 | 168 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 233 | 236 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 385 | 388 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 474 | 477 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 53 | 56 | PF00017 | 0.327 |
LIG_SH3_3 | 370 | 376 | PF00018 | 0.504 |
LIG_SH3_3 | 459 | 465 | PF00018 | 0.616 |
LIG_SH3_3 | 666 | 672 | PF00018 | 0.686 |
LIG_SH3_3 | 676 | 682 | PF00018 | 0.652 |
LIG_SH3_3 | 694 | 700 | PF00018 | 0.546 |
LIG_SUMO_SIM_anti_2 | 283 | 288 | PF11976 | 0.486 |
LIG_SUMO_SIM_par_1 | 507 | 513 | PF11976 | 0.352 |
LIG_TRAF2_1 | 375 | 378 | PF00917 | 0.512 |
LIG_TRAF2_1 | 522 | 525 | PF00917 | 0.503 |
LIG_TRAF2_1 | 541 | 544 | PF00917 | 0.422 |
LIG_TRAF2_1 | 88 | 91 | PF00917 | 0.527 |
LIG_TRAF2_2 | 620 | 625 | PF00917 | 0.719 |
LIG_TYR_ITIM | 163 | 168 | PF00017 | 0.315 |
MOD_CDK_SPxxK_3 | 584 | 591 | PF00069 | 0.710 |
MOD_CK1_1 | 201 | 207 | PF00069 | 0.496 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.592 |
MOD_CK1_1 | 311 | 317 | PF00069 | 0.621 |
MOD_CK1_1 | 397 | 403 | PF00069 | 0.647 |
MOD_CK1_1 | 417 | 423 | PF00069 | 0.692 |
MOD_CK1_1 | 464 | 470 | PF00069 | 0.488 |
MOD_CK1_1 | 570 | 576 | PF00069 | 0.739 |
MOD_CK1_1 | 664 | 670 | PF00069 | 0.629 |
MOD_CK2_1 | 85 | 91 | PF00069 | 0.560 |
MOD_CK2_1 | 92 | 98 | PF00069 | 0.550 |
MOD_Cter_Amidation | 358 | 361 | PF01082 | 0.636 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.642 |
MOD_GlcNHglycan | 18 | 21 | PF01048 | 0.545 |
MOD_GlcNHglycan | 309 | 313 | PF01048 | 0.631 |
MOD_GlcNHglycan | 387 | 390 | PF01048 | 0.570 |
MOD_GlcNHglycan | 407 | 410 | PF01048 | 0.738 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.470 |
MOD_GlcNHglycan | 425 | 428 | PF01048 | 0.643 |
MOD_GlcNHglycan | 480 | 483 | PF01048 | 0.404 |
MOD_GlcNHglycan | 617 | 620 | PF01048 | 0.734 |
MOD_GlcNHglycan | 625 | 629 | PF01048 | 0.498 |
MOD_GlcNHglycan | 637 | 640 | PF01048 | 0.632 |
MOD_GlcNHglycan | 664 | 667 | PF01048 | 0.619 |
MOD_GlcNHglycan | 675 | 678 | PF01048 | 0.641 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.526 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.694 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.457 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.680 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.742 |
MOD_GSK3_1 | 478 | 485 | PF00069 | 0.479 |
MOD_GSK3_1 | 604 | 611 | PF00069 | 0.670 |
MOD_GSK3_1 | 626 | 633 | PF00069 | 0.658 |
MOD_GSK3_1 | 664 | 671 | PF00069 | 0.642 |
MOD_GSK3_1 | 673 | 680 | PF00069 | 0.608 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.453 |
MOD_LATS_1 | 470 | 476 | PF00433 | 0.385 |
MOD_N-GLC_1 | 16 | 21 | PF02516 | 0.756 |
MOD_N-GLC_1 | 417 | 422 | PF02516 | 0.733 |
MOD_N-GLC_1 | 577 | 582 | PF02516 | 0.614 |
MOD_NEK2_1 | 243 | 248 | PF00069 | 0.398 |
MOD_NEK2_1 | 394 | 399 | PF00069 | 0.585 |
MOD_NEK2_1 | 478 | 483 | PF00069 | 0.461 |
MOD_NEK2_1 | 613 | 618 | PF00069 | 0.731 |
MOD_NEK2_2 | 51 | 56 | PF00069 | 0.410 |
MOD_NEK2_2 | 642 | 647 | PF00069 | 0.740 |
MOD_OFUCOSY | 133 | 138 | PF10250 | 0.410 |
MOD_OFUCOSY | 50 | 55 | PF10250 | 0.410 |
MOD_PIKK_1 | 532 | 538 | PF00454 | 0.571 |
MOD_PIKK_1 | 75 | 81 | PF00454 | 0.353 |
MOD_PKA_2 | 199 | 205 | PF00069 | 0.540 |
MOD_PKA_2 | 414 | 420 | PF00069 | 0.737 |
MOD_PKA_2 | 66 | 72 | PF00069 | 0.246 |
MOD_Plk_1 | 198 | 204 | PF00069 | 0.482 |
MOD_Plk_1 | 692 | 698 | PF00069 | 0.662 |
MOD_Plk_1 | 75 | 81 | PF00069 | 0.306 |
MOD_Plk_4 | 220 | 226 | PF00069 | 0.435 |
MOD_Plk_4 | 664 | 670 | PF00069 | 0.552 |
MOD_ProDKin_1 | 115 | 121 | PF00069 | 0.469 |
MOD_ProDKin_1 | 22 | 28 | PF00069 | 0.636 |
MOD_ProDKin_1 | 300 | 306 | PF00069 | 0.587 |
MOD_ProDKin_1 | 461 | 467 | PF00069 | 0.535 |
MOD_ProDKin_1 | 578 | 584 | PF00069 | 0.753 |
MOD_ProDKin_1 | 668 | 674 | PF00069 | 0.719 |
MOD_ProDKin_1 | 678 | 684 | PF00069 | 0.664 |
MOD_SUMO_rev_2 | 545 | 555 | PF00179 | 0.545 |
TRG_DiLeu_LyEn_5 | 505 | 510 | PF01217 | 0.285 |
TRG_ENDOCYTIC_2 | 165 | 168 | PF00928 | 0.315 |
TRG_ENDOCYTIC_2 | 468 | 471 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 488 | 491 | PF00928 | 0.309 |
TRG_ER_diArg_1 | 102 | 104 | PF00400 | 0.482 |
TRG_ER_diArg_1 | 704 | 706 | PF00400 | 0.707 |
TRG_NES_CRM1_1 | 149 | 162 | PF08389 | 0.429 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IA72 | Leptomonas seymouri | 65% | 100% |
A0A0S4KKN7 | Bodo saltans | 39% | 100% |
A0A1X0P1Y0 | Trypanosomatidae | 43% | 100% |
A0A3S7X380 | Leishmania donovani | 100% | 100% |
A0A422P542 | Trypanosoma rangeli | 40% | 100% |
A4HI75 | Leishmania braziliensis | 81% | 100% |
E9B0Q2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
Q4Q7I1 | Leishmania major | 94% | 100% |
V5BYZ6 | Trypanosoma cruzi | 36% | 100% |