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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: E9B5Z6
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0004792 | thiosulfate sulfurtransferase activity | 5 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0016782 | transferase activity, transferring sulphur-containing groups | 3 | 1 |
GO:0016783 | sulfurtransferase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 116 | 120 | PF00656 | 0.568 |
CLV_C14_Caspase3-7 | 139 | 143 | PF00656 | 0.561 |
CLV_C14_Caspase3-7 | 193 | 197 | PF00656 | 0.668 |
CLV_C14_Caspase3-7 | 575 | 579 | PF00656 | 0.560 |
CLV_NRD_NRD_1 | 135 | 137 | PF00675 | 0.489 |
CLV_NRD_NRD_1 | 235 | 237 | PF00675 | 0.429 |
CLV_NRD_NRD_1 | 430 | 432 | PF00675 | 0.537 |
CLV_NRD_NRD_1 | 444 | 446 | PF00675 | 0.543 |
CLV_NRD_NRD_1 | 537 | 539 | PF00675 | 0.738 |
CLV_NRD_NRD_1 | 602 | 604 | PF00675 | 0.735 |
CLV_NRD_NRD_1 | 76 | 78 | PF00675 | 0.740 |
CLV_PCSK_FUR_1 | 535 | 539 | PF00082 | 0.632 |
CLV_PCSK_KEX2_1 | 135 | 137 | PF00082 | 0.489 |
CLV_PCSK_KEX2_1 | 235 | 237 | PF00082 | 0.427 |
CLV_PCSK_KEX2_1 | 430 | 432 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 444 | 446 | PF00082 | 0.527 |
CLV_PCSK_KEX2_1 | 537 | 539 | PF00082 | 0.680 |
CLV_PCSK_KEX2_1 | 602 | 604 | PF00082 | 0.735 |
CLV_PCSK_KEX2_1 | 76 | 78 | PF00082 | 0.740 |
CLV_PCSK_SKI1_1 | 255 | 259 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 318 | 322 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 445 | 449 | PF00082 | 0.579 |
CLV_PCSK_SKI1_1 | 562 | 566 | PF00082 | 0.618 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.720 |
DEG_SPOP_SBC_1 | 145 | 149 | PF00917 | 0.688 |
DEG_SPOP_SBC_1 | 168 | 172 | PF00917 | 0.674 |
DEG_SPOP_SBC_1 | 295 | 299 | PF00917 | 0.651 |
DOC_MAPK_gen_1 | 379 | 387 | PF00069 | 0.490 |
DOC_MAPK_MEF2A_6 | 558 | 567 | PF00069 | 0.630 |
DOC_PP4_FxxP_1 | 377 | 380 | PF00568 | 0.480 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 145 | 149 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 168 | 172 | PF00917 | 0.759 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.599 |
DOC_USP7_MATH_1 | 287 | 291 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 522 | 526 | PF00917 | 0.716 |
DOC_USP7_MATH_1 | 528 | 532 | PF00917 | 0.755 |
DOC_USP7_MATH_1 | 7 | 11 | PF00917 | 0.706 |
DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.801 |
DOC_USP7_UBL2_3 | 243 | 247 | PF12436 | 0.476 |
DOC_USP7_UBL2_3 | 37 | 41 | PF12436 | 0.696 |
DOC_USP7_UBL2_3 | 497 | 501 | PF12436 | 0.587 |
DOC_WW_Pin1_4 | 170 | 175 | PF00397 | 0.731 |
DOC_WW_Pin1_4 | 24 | 29 | PF00397 | 0.682 |
DOC_WW_Pin1_4 | 478 | 483 | PF00397 | 0.573 |
DOC_WW_Pin1_4 | 586 | 591 | PF00397 | 0.687 |
DOC_WW_Pin1_4 | 592 | 597 | PF00397 | 0.726 |
LIG_14-3-3_CanoR_1 | 444 | 450 | PF00244 | 0.584 |
LIG_14-3-3_CanoR_1 | 562 | 568 | PF00244 | 0.647 |
LIG_14-3-3_CanoR_1 | 91 | 97 | PF00244 | 0.713 |
LIG_Actin_WH2_2 | 266 | 284 | PF00022 | 0.528 |
LIG_BRCT_BRCA1_1 | 147 | 151 | PF00533 | 0.707 |
LIG_eIF4E_1 | 392 | 398 | PF01652 | 0.477 |
LIG_FHA_1 | 256 | 262 | PF00498 | 0.591 |
LIG_FHA_1 | 38 | 44 | PF00498 | 0.705 |
LIG_FHA_1 | 501 | 507 | PF00498 | 0.479 |
LIG_FHA_1 | 534 | 540 | PF00498 | 0.642 |
LIG_FHA_1 | 543 | 549 | PF00498 | 0.592 |
LIG_FHA_1 | 592 | 598 | PF00498 | 0.718 |
LIG_FHA_1 | 70 | 76 | PF00498 | 0.619 |
LIG_FHA_2 | 182 | 188 | PF00498 | 0.738 |
LIG_FHA_2 | 191 | 197 | PF00498 | 0.637 |
LIG_FHA_2 | 207 | 213 | PF00498 | 0.614 |
LIG_FHA_2 | 239 | 245 | PF00498 | 0.541 |
LIG_FHA_2 | 258 | 264 | PF00498 | 0.342 |
LIG_FHA_2 | 295 | 301 | PF00498 | 0.579 |
LIG_FHA_2 | 322 | 328 | PF00498 | 0.478 |
LIG_FHA_2 | 337 | 343 | PF00498 | 0.428 |
LIG_FHA_2 | 550 | 556 | PF00498 | 0.700 |
LIG_FHA_2 | 573 | 579 | PF00498 | 0.617 |
LIG_LIR_Apic_2 | 204 | 208 | PF02991 | 0.640 |
LIG_LIR_Apic_2 | 374 | 380 | PF02991 | 0.479 |
LIG_LIR_Gen_1 | 329 | 340 | PF02991 | 0.320 |
LIG_LIR_Gen_1 | 359 | 368 | PF02991 | 0.477 |
LIG_LIR_Gen_1 | 462 | 471 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 329 | 335 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 344 | 349 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 359 | 364 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 404 | 408 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 462 | 466 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 494 | 499 | PF02991 | 0.542 |
LIG_PCNA_yPIPBox_3 | 423 | 433 | PF02747 | 0.492 |
LIG_Pex14_1 | 421 | 425 | PF04695 | 0.548 |
LIG_SH2_CRK | 425 | 429 | PF00017 | 0.476 |
LIG_SH2_CRK | 496 | 500 | PF00017 | 0.538 |
LIG_SH2_SRC | 328 | 331 | PF00017 | 0.423 |
LIG_SH2_STAT5 | 389 | 392 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 408 | 411 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 474 | 477 | PF00017 | 0.641 |
LIG_SH3_1 | 41 | 47 | PF00018 | 0.498 |
LIG_SH3_3 | 200 | 206 | PF00018 | 0.647 |
LIG_SH3_3 | 262 | 268 | PF00018 | 0.528 |
LIG_SH3_3 | 41 | 47 | PF00018 | 0.603 |
LIG_TRAF2_1 | 129 | 132 | PF00917 | 0.613 |
LIG_TRAF2_1 | 314 | 317 | PF00917 | 0.550 |
LIG_TRAF2_1 | 367 | 370 | PF00917 | 0.556 |
LIG_TRAF2_1 | 467 | 470 | PF00917 | 0.527 |
LIG_UBA3_1 | 402 | 410 | PF00899 | 0.520 |
LIG_WRC_WIRS_1 | 446 | 451 | PF05994 | 0.581 |
LIG_WW_3 | 599 | 603 | PF00397 | 0.759 |
MOD_CDC14_SPxK_1 | 481 | 484 | PF00782 | 0.619 |
MOD_CDK_SPK_2 | 24 | 29 | PF00069 | 0.682 |
MOD_CDK_SPxK_1 | 478 | 484 | PF00069 | 0.623 |
MOD_CDK_SPxxK_3 | 170 | 177 | PF00069 | 0.671 |
MOD_CDK_SPxxK_3 | 586 | 593 | PF00069 | 0.707 |
MOD_CK1_1 | 147 | 153 | PF00069 | 0.787 |
MOD_CK1_1 | 531 | 537 | PF00069 | 0.644 |
MOD_CK1_1 | 595 | 601 | PF00069 | 0.805 |
MOD_CK1_1 | 93 | 99 | PF00069 | 0.701 |
MOD_CK2_1 | 147 | 153 | PF00069 | 0.491 |
MOD_CK2_1 | 238 | 244 | PF00069 | 0.540 |
MOD_CK2_1 | 257 | 263 | PF00069 | 0.344 |
MOD_CK2_1 | 294 | 300 | PF00069 | 0.681 |
MOD_CK2_1 | 311 | 317 | PF00069 | 0.321 |
MOD_CK2_1 | 321 | 327 | PF00069 | 0.438 |
MOD_CK2_1 | 336 | 342 | PF00069 | 0.477 |
MOD_CK2_1 | 436 | 442 | PF00069 | 0.580 |
MOD_CK2_1 | 98 | 104 | PF00069 | 0.691 |
MOD_Cter_Amidation | 35 | 38 | PF01082 | 0.619 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.720 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.675 |
MOD_GlcNHglycan | 164 | 167 | PF01048 | 0.682 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.720 |
MOD_GlcNHglycan | 291 | 294 | PF01048 | 0.720 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.645 |
MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.436 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.570 |
MOD_GlcNHglycan | 438 | 441 | PF01048 | 0.532 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.781 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.775 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.644 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.559 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.727 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.636 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.494 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.472 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.568 |
MOD_GSK3_1 | 572 | 579 | PF00069 | 0.537 |
MOD_GSK3_1 | 591 | 598 | PF00069 | 0.812 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.808 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.709 |
MOD_N-GLC_1 | 113 | 118 | PF02516 | 0.608 |
MOD_N-GLC_1 | 190 | 195 | PF02516 | 0.744 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.729 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.686 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.670 |
MOD_NEK2_1 | 224 | 229 | PF00069 | 0.462 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.366 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.662 |
MOD_NEK2_1 | 320 | 325 | PF00069 | 0.438 |
MOD_NEK2_1 | 475 | 480 | PF00069 | 0.576 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.741 |
MOD_PIKK_1 | 528 | 534 | PF00454 | 0.675 |
MOD_PIKK_1 | 595 | 601 | PF00454 | 0.528 |
MOD_PKA_1 | 255 | 261 | PF00069 | 0.422 |
MOD_PKA_1 | 37 | 43 | PF00069 | 0.611 |
MOD_PKA_2 | 475 | 481 | PF00069 | 0.636 |
MOD_PKA_2 | 78 | 84 | PF00069 | 0.670 |
MOD_PKA_2 | 90 | 96 | PF00069 | 0.658 |
MOD_PKB_1 | 77 | 85 | PF00069 | 0.655 |
MOD_Plk_1 | 113 | 119 | PF00069 | 0.576 |
MOD_Plk_1 | 190 | 196 | PF00069 | 0.746 |
MOD_Plk_1 | 213 | 219 | PF00069 | 0.486 |
MOD_Plk_1 | 341 | 347 | PF00069 | 0.477 |
MOD_Plk_1 | 93 | 99 | PF00069 | 0.546 |
MOD_Plk_2-3 | 336 | 342 | PF00069 | 0.477 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.527 |
MOD_Plk_4 | 224 | 230 | PF00069 | 0.472 |
MOD_Plk_4 | 401 | 407 | PF00069 | 0.477 |
MOD_Plk_4 | 572 | 578 | PF00069 | 0.576 |
MOD_ProDKin_1 | 170 | 176 | PF00069 | 0.728 |
MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.683 |
MOD_ProDKin_1 | 478 | 484 | PF00069 | 0.574 |
MOD_ProDKin_1 | 586 | 592 | PF00069 | 0.689 |
MOD_SUMO_for_1 | 556 | 559 | PF00179 | 0.565 |
MOD_SUMO_rev_2 | 311 | 320 | PF00179 | 0.499 |
MOD_SUMO_rev_2 | 585 | 595 | PF00179 | 0.732 |
TRG_DiLeu_BaEn_1 | 316 | 321 | PF01217 | 0.498 |
TRG_DiLeu_BaEn_4 | 132 | 138 | PF01217 | 0.576 |
TRG_DiLeu_BaEn_4 | 316 | 322 | PF01217 | 0.549 |
TRG_ENDOCYTIC_2 | 408 | 411 | PF00928 | 0.484 |
TRG_ENDOCYTIC_2 | 425 | 428 | PF00928 | 0.537 |
TRG_ENDOCYTIC_2 | 496 | 499 | PF00928 | 0.541 |
TRG_ER_diArg_1 | 134 | 136 | PF00400 | 0.481 |
TRG_ER_diArg_1 | 229 | 232 | PF00400 | 0.408 |
TRG_ER_diArg_1 | 234 | 236 | PF00400 | 0.420 |
TRG_ER_diArg_1 | 429 | 431 | PF00400 | 0.523 |
TRG_ER_diArg_1 | 443 | 445 | PF00400 | 0.534 |
TRG_ER_diArg_1 | 535 | 538 | PF00400 | 0.691 |
TRG_ER_diArg_1 | 601 | 603 | PF00400 | 0.719 |
TRG_ER_diArg_1 | 75 | 77 | PF00400 | 0.770 |
TRG_NES_CRM1_1 | 458 | 470 | PF08389 | 0.516 |
TRG_Pf-PMV_PEXEL_1 | 135 | 139 | PF00026 | 0.492 |
TRG_Pf-PMV_PEXEL_1 | 215 | 219 | PF00026 | 0.471 |
TRG_Pf-PMV_PEXEL_1 | 232 | 237 | PF00026 | 0.416 |
TRG_Pf-PMV_PEXEL_1 | 537 | 541 | PF00026 | 0.614 |
TRG_Pf-PMV_PEXEL_1 | 546 | 550 | PF00026 | 0.589 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5U9 | Leptomonas seymouri | 64% | 100% |
A0A0S4IZW5 | Bodo saltans | 46% | 100% |
A0A3Q8IEZ4 | Leishmania donovani | 89% | 99% |
A4HMD8 | Leishmania braziliensis | 77% | 99% |
A4IB11 | Leishmania infantum | 89% | 99% |
E9AEU0 | Leishmania major | 89% | 100% |