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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A4HGF5
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0004842 | ubiquitin-protein transferase activity | 4 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0008270 | zinc ion binding | 6 | 7 |
GO:0016740 | transferase activity | 2 | 7 |
GO:0019787 | ubiquitin-like protein transferase activity | 3 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043169 | cation binding | 3 | 7 |
GO:0046872 | metal ion binding | 4 | 7 |
GO:0046914 | transition metal ion binding | 5 | 7 |
GO:0061630 | ubiquitin protein ligase activity | 5 | 7 |
GO:0061659 | ubiquitin-like protein ligase activity | 4 | 7 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 369 | 373 | PF00656 | 0.674 |
CLV_C14_Caspase3-7 | 506 | 510 | PF00656 | 0.602 |
CLV_NRD_NRD_1 | 245 | 247 | PF00675 | 0.750 |
CLV_NRD_NRD_1 | 456 | 458 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 849 | 851 | PF00675 | 0.703 |
CLV_PCSK_KEX2_1 | 247 | 249 | PF00082 | 0.757 |
CLV_PCSK_KEX2_1 | 258 | 260 | PF00082 | 0.758 |
CLV_PCSK_KEX2_1 | 349 | 351 | PF00082 | 0.847 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.664 |
CLV_PCSK_KEX2_1 | 456 | 458 | PF00082 | 0.483 |
CLV_PCSK_PC1ET2_1 | 247 | 249 | PF00082 | 0.757 |
CLV_PCSK_PC1ET2_1 | 258 | 260 | PF00082 | 0.758 |
CLV_PCSK_PC1ET2_1 | 349 | 351 | PF00082 | 0.847 |
CLV_PCSK_PC1ET2_1 | 4 | 6 | PF00082 | 0.625 |
CLV_PCSK_PC7_1 | 243 | 249 | PF00082 | 0.748 |
CLV_PCSK_SKI1_1 | 49 | 53 | PF00082 | 0.632 |
CLV_PCSK_SKI1_1 | 596 | 600 | PF00082 | 0.669 |
CLV_PCSK_SKI1_1 | 643 | 647 | PF00082 | 0.634 |
CLV_PCSK_SKI1_1 | 673 | 677 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 71 | 75 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 835 | 839 | PF00082 | 0.514 |
DEG_SCF_FBW7_1 | 254 | 260 | PF00400 | 0.752 |
DEG_SPOP_SBC_1 | 249 | 253 | PF00917 | 0.754 |
DEG_SPOP_SBC_1 | 286 | 290 | PF00917 | 0.588 |
DOC_CKS1_1 | 254 | 259 | PF01111 | 0.696 |
DOC_CYCLIN_RxL_1 | 66 | 77 | PF00134 | 0.622 |
DOC_CYCLIN_yCln2_LP_2 | 22 | 28 | PF00134 | 0.607 |
DOC_CYCLIN_yCln2_LP_2 | 72 | 78 | PF00134 | 0.366 |
DOC_MAPK_gen_1 | 14 | 22 | PF00069 | 0.543 |
DOC_MAPK_gen_1 | 4 | 11 | PF00069 | 0.504 |
DOC_MAPK_gen_1 | 47 | 56 | PF00069 | 0.543 |
DOC_MAPK_HePTP_8 | 44 | 56 | PF00069 | 0.390 |
DOC_MAPK_MEF2A_6 | 17 | 24 | PF00069 | 0.527 |
DOC_MAPK_MEF2A_6 | 47 | 56 | PF00069 | 0.538 |
DOC_MAPK_NFAT4_5 | 47 | 55 | PF00069 | 0.541 |
DOC_PP1_RVXF_1 | 69 | 75 | PF00149 | 0.606 |
DOC_PP2B_LxvP_1 | 22 | 25 | PF13499 | 0.602 |
DOC_PP2B_LxvP_1 | 52 | 55 | PF13499 | 0.553 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.727 |
DOC_USP7_MATH_1 | 225 | 229 | PF00917 | 0.769 |
DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.793 |
DOC_USP7_MATH_1 | 297 | 301 | PF00917 | 0.685 |
DOC_USP7_MATH_1 | 311 | 315 | PF00917 | 0.734 |
DOC_USP7_MATH_1 | 396 | 400 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 422 | 426 | PF00917 | 0.602 |
DOC_USP7_MATH_1 | 718 | 722 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 750 | 754 | PF00917 | 0.621 |
DOC_USP7_MATH_2 | 75 | 81 | PF00917 | 0.380 |
DOC_WW_Pin1_4 | 221 | 226 | PF00397 | 0.743 |
DOC_WW_Pin1_4 | 250 | 255 | PF00397 | 0.701 |
DOC_WW_Pin1_4 | 261 | 266 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 319 | 324 | PF00397 | 0.699 |
DOC_WW_Pin1_4 | 348 | 353 | PF00397 | 0.773 |
DOC_WW_Pin1_4 | 602 | 607 | PF00397 | 0.530 |
LIG_14-3-3_CanoR_1 | 119 | 127 | PF00244 | 0.648 |
LIG_14-3-3_CanoR_1 | 133 | 137 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 248 | 254 | PF00244 | 0.725 |
LIG_14-3-3_CanoR_1 | 270 | 276 | PF00244 | 0.636 |
LIG_14-3-3_CanoR_1 | 449 | 454 | PF00244 | 0.574 |
LIG_14-3-3_CanoR_1 | 517 | 525 | PF00244 | 0.500 |
LIG_14-3-3_CanoR_1 | 652 | 660 | PF00244 | 0.680 |
LIG_AP2alpha_2 | 412 | 414 | PF02296 | 0.681 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.618 |
LIG_BRCT_BRCA1_1 | 312 | 316 | PF00533 | 0.818 |
LIG_BRCT_BRCA1_1 | 615 | 619 | PF00533 | 0.669 |
LIG_BRCT_BRCA1_1 | 769 | 773 | PF00533 | 0.587 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.657 |
LIG_FHA_1 | 142 | 148 | PF00498 | 0.498 |
LIG_FHA_1 | 250 | 256 | PF00498 | 0.753 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.619 |
LIG_FHA_1 | 39 | 45 | PF00498 | 0.392 |
LIG_FHA_1 | 559 | 565 | PF00498 | 0.483 |
LIG_FHA_1 | 656 | 662 | PF00498 | 0.632 |
LIG_FHA_1 | 691 | 697 | PF00498 | 0.605 |
LIG_FHA_2 | 121 | 127 | PF00498 | 0.612 |
LIG_FHA_2 | 148 | 154 | PF00498 | 0.508 |
LIG_FHA_2 | 27 | 33 | PF00498 | 0.623 |
LIG_FHA_2 | 506 | 512 | PF00498 | 0.443 |
LIG_FHA_2 | 739 | 745 | PF00498 | 0.575 |
LIG_FHA_2 | 826 | 832 | PF00498 | 0.532 |
LIG_GBD_Chelix_1 | 814 | 822 | PF00786 | 0.683 |
LIG_IBAR_NPY_1 | 421 | 423 | PF08397 | 0.472 |
LIG_KLC1_Yacidic_2 | 6 | 10 | PF13176 | 0.480 |
LIG_LIR_Gen_1 | 6 | 15 | PF02991 | 0.489 |
LIG_LIR_Gen_1 | 644 | 651 | PF02991 | 0.668 |
LIG_LIR_Gen_1 | 775 | 784 | PF02991 | 0.683 |
LIG_LIR_Nem_3 | 540 | 546 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 558 | 563 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 6 | 11 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 644 | 649 | PF02991 | 0.675 |
LIG_LIR_Nem_3 | 775 | 781 | PF02991 | 0.672 |
LIG_Pex14_1 | 180 | 184 | PF04695 | 0.676 |
LIG_Pex14_2 | 7 | 11 | PF04695 | 0.469 |
LIG_PTB_Apo_2 | 554 | 561 | PF02174 | 0.392 |
LIG_REV1ctd_RIR_1 | 692 | 702 | PF16727 | 0.610 |
LIG_SH2_STAP1 | 765 | 769 | PF00017 | 0.536 |
LIG_SH2_STAT3 | 140 | 143 | PF00017 | 0.554 |
LIG_SH2_STAT3 | 567 | 570 | PF00017 | 0.588 |
LIG_SH2_STAT3 | 584 | 587 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 140 | 143 | PF00017 | 0.518 |
LIG_SH2_STAT5 | 146 | 149 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 418 | 421 | PF00017 | 0.620 |
LIG_SH2_STAT5 | 567 | 570 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 8 | 11 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 800 | 803 | PF00017 | 0.650 |
LIG_SH3_2 | 254 | 259 | PF14604 | 0.754 |
LIG_SH3_3 | 196 | 202 | PF00018 | 0.727 |
LIG_SH3_3 | 219 | 225 | PF00018 | 0.580 |
LIG_SH3_3 | 251 | 257 | PF00018 | 0.751 |
LIG_SH3_3 | 317 | 323 | PF00018 | 0.736 |
LIG_SH3_3 | 407 | 413 | PF00018 | 0.725 |
LIG_SH3_3 | 478 | 484 | PF00018 | 0.457 |
LIG_SH3_3 | 723 | 729 | PF00018 | 0.676 |
LIG_SUMO_SIM_par_1 | 18 | 23 | PF11976 | 0.530 |
LIG_SUMO_SIM_par_1 | 224 | 230 | PF11976 | 0.554 |
LIG_SUMO_SIM_par_1 | 377 | 382 | PF11976 | 0.519 |
LIG_TRAF2_1 | 302 | 305 | PF00917 | 0.580 |
LIG_UBA3_1 | 50 | 58 | PF00899 | 0.547 |
MOD_CDC14_SPxK_1 | 351 | 354 | PF00782 | 0.570 |
MOD_CDK_SPK_2 | 253 | 258 | PF00069 | 0.753 |
MOD_CDK_SPxK_1 | 253 | 259 | PF00069 | 0.755 |
MOD_CDK_SPxK_1 | 348 | 354 | PF00069 | 0.763 |
MOD_CK1_1 | 115 | 121 | PF00069 | 0.665 |
MOD_CK1_1 | 221 | 227 | PF00069 | 0.723 |
MOD_CK1_1 | 260 | 266 | PF00069 | 0.758 |
MOD_CK1_1 | 287 | 293 | PF00069 | 0.672 |
MOD_CK1_1 | 300 | 306 | PF00069 | 0.684 |
MOD_CK1_1 | 629 | 635 | PF00069 | 0.404 |
MOD_CK1_1 | 653 | 659 | PF00069 | 0.675 |
MOD_CK2_1 | 120 | 126 | PF00069 | 0.612 |
MOD_CK2_1 | 235 | 241 | PF00069 | 0.632 |
MOD_CK2_1 | 653 | 659 | PF00069 | 0.635 |
MOD_CK2_1 | 718 | 724 | PF00069 | 0.555 |
MOD_CK2_1 | 77 | 83 | PF00069 | 0.379 |
MOD_CK2_1 | 825 | 831 | PF00069 | 0.542 |
MOD_Cter_Amidation | 347 | 350 | PF01082 | 0.844 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.578 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.471 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.749 |
MOD_GlcNHglycan | 289 | 292 | PF01048 | 0.625 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.766 |
MOD_GlcNHglycan | 609 | 612 | PF01048 | 0.646 |
MOD_GlcNHglycan | 628 | 631 | PF01048 | 0.327 |
MOD_GlcNHglycan | 655 | 658 | PF01048 | 0.639 |
MOD_GlcNHglycan | 752 | 755 | PF01048 | 0.714 |
MOD_GlcNHglycan | 95 | 98 | PF01048 | 0.532 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.658 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.689 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.694 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.695 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.623 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.595 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.585 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.774 |
MOD_GSK3_1 | 396 | 403 | PF00069 | 0.798 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.524 |
MOD_GSK3_1 | 445 | 452 | PF00069 | 0.496 |
MOD_GSK3_1 | 501 | 508 | PF00069 | 0.497 |
MOD_GSK3_1 | 629 | 636 | PF00069 | 0.489 |
MOD_GSK3_1 | 651 | 658 | PF00069 | 0.709 |
MOD_GSK3_1 | 814 | 821 | PF00069 | 0.681 |
MOD_N-GLC_1 | 750 | 755 | PF02516 | 0.622 |
MOD_N-GLC_2 | 415 | 417 | PF02516 | 0.590 |
MOD_N-GLC_2 | 475 | 477 | PF02516 | 0.364 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.612 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.518 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.525 |
MOD_NEK2_1 | 216 | 221 | PF00069 | 0.532 |
MOD_NEK2_1 | 379 | 384 | PF00069 | 0.520 |
MOD_NEK2_1 | 437 | 442 | PF00069 | 0.534 |
MOD_NEK2_1 | 466 | 471 | PF00069 | 0.608 |
MOD_NEK2_1 | 690 | 695 | PF00069 | 0.553 |
MOD_NEK2_1 | 814 | 819 | PF00069 | 0.684 |
MOD_NEK2_1 | 93 | 98 | PF00069 | 0.370 |
MOD_NEK2_2 | 26 | 31 | PF00069 | 0.516 |
MOD_NEK2_2 | 280 | 285 | PF00069 | 0.602 |
MOD_NEK2_2 | 641 | 646 | PF00069 | 0.362 |
MOD_NEK2_2 | 671 | 676 | PF00069 | 0.558 |
MOD_OFUCOSY | 435 | 441 | PF10250 | 0.521 |
MOD_OFUCOSY | 474 | 480 | PF10250 | 0.324 |
MOD_PIKK_1 | 189 | 195 | PF00454 | 0.646 |
MOD_PIKK_1 | 227 | 233 | PF00454 | 0.559 |
MOD_PIKK_1 | 300 | 306 | PF00454 | 0.839 |
MOD_PIKK_1 | 816 | 822 | PF00454 | 0.679 |
MOD_PKA_2 | 132 | 138 | PF00069 | 0.568 |
MOD_PKA_2 | 141 | 147 | PF00069 | 0.511 |
MOD_PKA_2 | 242 | 248 | PF00069 | 0.759 |
MOD_PKA_2 | 260 | 266 | PF00069 | 0.562 |
MOD_PKA_2 | 269 | 275 | PF00069 | 0.522 |
MOD_PKA_2 | 300 | 306 | PF00069 | 0.745 |
MOD_PKA_2 | 500 | 506 | PF00069 | 0.518 |
MOD_PKA_2 | 516 | 522 | PF00069 | 0.513 |
MOD_PKA_2 | 651 | 657 | PF00069 | 0.751 |
MOD_PKA_2 | 718 | 724 | PF00069 | 0.586 |
MOD_PKB_1 | 246 | 254 | PF00069 | 0.754 |
MOD_Plk_1 | 115 | 121 | PF00069 | 0.638 |
MOD_Plk_1 | 280 | 286 | PF00069 | 0.671 |
MOD_Plk_1 | 304 | 310 | PF00069 | 0.585 |
MOD_Plk_1 | 38 | 44 | PF00069 | 0.543 |
MOD_Plk_1 | 495 | 501 | PF00069 | 0.390 |
MOD_Plk_1 | 538 | 544 | PF00069 | 0.679 |
MOD_Plk_1 | 690 | 696 | PF00069 | 0.560 |
MOD_Plk_1 | 774 | 780 | PF00069 | 0.577 |
MOD_Plk_1 | 835 | 841 | PF00069 | 0.518 |
MOD_Plk_2-3 | 505 | 511 | PF00069 | 0.462 |
MOD_Plk_2-3 | 539 | 545 | PF00069 | 0.674 |
MOD_Plk_4 | 15 | 21 | PF00069 | 0.523 |
MOD_Plk_4 | 342 | 348 | PF00069 | 0.570 |
MOD_Plk_4 | 396 | 402 | PF00069 | 0.715 |
MOD_Plk_4 | 495 | 501 | PF00069 | 0.522 |
MOD_Plk_4 | 65 | 71 | PF00069 | 0.629 |
MOD_Plk_4 | 690 | 696 | PF00069 | 0.543 |
MOD_Plk_4 | 835 | 841 | PF00069 | 0.518 |
MOD_ProDKin_1 | 221 | 227 | PF00069 | 0.744 |
MOD_ProDKin_1 | 250 | 256 | PF00069 | 0.702 |
MOD_ProDKin_1 | 261 | 267 | PF00069 | 0.677 |
MOD_ProDKin_1 | 319 | 325 | PF00069 | 0.702 |
MOD_ProDKin_1 | 348 | 354 | PF00069 | 0.772 |
MOD_ProDKin_1 | 602 | 608 | PF00069 | 0.532 |
MOD_SUMO_for_1 | 3 | 6 | PF00179 | 0.639 |
MOD_SUMO_rev_2 | 32 | 41 | PF00179 | 0.417 |
MOD_SUMO_rev_2 | 6 | 15 | PF00179 | 0.489 |
TRG_DiLeu_BaEn_1 | 116 | 121 | PF01217 | 0.638 |
TRG_DiLeu_BaEn_1 | 305 | 310 | PF01217 | 0.584 |
TRG_DiLeu_BaLyEn_6 | 374 | 379 | PF01217 | 0.533 |
TRG_DiLeu_BaLyEn_6 | 46 | 51 | PF01217 | 0.637 |
TRG_DiLeu_BaLyEn_6 | 68 | 73 | PF01217 | 0.527 |
TRG_DiLeu_LyEn_5 | 305 | 310 | PF01217 | 0.584 |
TRG_ENDOCYTIC_2 | 455 | 458 | PF00928 | 0.451 |
TRG_ENDOCYTIC_2 | 461 | 464 | PF00928 | 0.441 |
TRG_ENDOCYTIC_2 | 621 | 624 | PF00928 | 0.521 |
TRG_ENDOCYTIC_2 | 8 | 11 | PF00928 | 0.471 |
TRG_ER_diArg_1 | 455 | 457 | PF00400 | 0.479 |
TRG_NES_CRM1_1 | 779 | 791 | PF08389 | 0.605 |
TRG_NLS_Bipartite_1 | 246 | 262 | PF00514 | 0.754 |
TRG_NLS_MonoExtC_3 | 245 | 250 | PF00514 | 0.754 |
TRG_NLS_MonoExtN_4 | 243 | 250 | PF00514 | 0.749 |
TRG_NLS_MonoExtN_4 | 257 | 262 | PF00514 | 0.754 |
TRG_Pf-PMV_PEXEL_1 | 704 | 709 | PF00026 | 0.628 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HU94 | Leptomonas seymouri | 60% | 100% |
A0A3S7X1F3 | Leishmania donovani | 79% | 100% |
A4I3I6 | Leishmania infantum | 79% | 100% |
E9AZS8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 100% |
Q4Q8F6 | Leishmania major | 79% | 100% |