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:0005737 | cytoplasm | 2 | 1 |
GO:0005829 | cytosol | 2 | 1 |
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0031981 | nuclear lumen | 5 | 1 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
GO:0097014 | ciliary plasm | 5 | 1 |
GO:0099568 | cytoplasmic region | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AJV8
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 10 |
GO:0016787 | hydrolase activity | 2 | 10 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 10 |
GO:0004518 | nuclease activity | 4 | 1 |
GO:0004527 | exonuclease activity | 5 | 1 |
GO:0004529 | DNA exonuclease activity | 5 | 1 |
GO:0004536 | DNA nuclease activity | 4 | 1 |
GO:0008296 | 3'-5'-DNA exonuclease activity | 7 | 1 |
GO:0008297 | single-stranded DNA exodeoxyribonuclease activity | 7 | 1 |
GO:0008310 | single-stranded DNA 3'-5' DNA exonuclease activity | 8 | 1 |
GO:0008408 | 3'-5' exonuclease activity | 6 | 1 |
GO:0016796 | exonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters | 6 | 1 |
GO:0016895 | DNA exonuclease activity, producing 5'-phosphomonoesters | 6 | 1 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 1 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 308 | 312 | PF00656 | 0.373 |
CLV_C14_Caspase3-7 | 402 | 406 | PF00656 | 0.471 |
CLV_C14_Caspase3-7 | 519 | 523 | PF00656 | 0.420 |
CLV_C14_Caspase3-7 | 608 | 612 | PF00656 | 0.702 |
CLV_C14_Caspase3-7 | 692 | 696 | PF00656 | 0.671 |
CLV_NRD_NRD_1 | 109 | 111 | PF00675 | 0.249 |
CLV_NRD_NRD_1 | 121 | 123 | PF00675 | 0.249 |
CLV_NRD_NRD_1 | 18 | 20 | PF00675 | 0.627 |
CLV_NRD_NRD_1 | 546 | 548 | PF00675 | 0.525 |
CLV_NRD_NRD_1 | 568 | 570 | PF00675 | 0.510 |
CLV_PCSK_FUR_1 | 564 | 568 | PF00082 | 0.551 |
CLV_PCSK_KEX2_1 | 121 | 123 | PF00082 | 0.332 |
CLV_PCSK_KEX2_1 | 18 | 20 | PF00082 | 0.699 |
CLV_PCSK_KEX2_1 | 35 | 37 | PF00082 | 0.532 |
CLV_PCSK_KEX2_1 | 524 | 526 | PF00082 | 0.562 |
CLV_PCSK_KEX2_1 | 545 | 547 | PF00082 | 0.575 |
CLV_PCSK_KEX2_1 | 563 | 565 | PF00082 | 0.450 |
CLV_PCSK_KEX2_1 | 566 | 568 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 598 | 600 | PF00082 | 0.502 |
CLV_PCSK_PC1ET2_1 | 35 | 37 | PF00082 | 0.530 |
CLV_PCSK_PC1ET2_1 | 524 | 526 | PF00082 | 0.562 |
CLV_PCSK_PC1ET2_1 | 563 | 565 | PF00082 | 0.459 |
CLV_PCSK_PC1ET2_1 | 566 | 568 | PF00082 | 0.475 |
CLV_PCSK_PC1ET2_1 | 598 | 600 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 10 | 14 | PF00082 | 0.625 |
CLV_PCSK_SKI1_1 | 165 | 169 | PF00082 | 0.246 |
CLV_PCSK_SKI1_1 | 260 | 264 | PF00082 | 0.307 |
CLV_PCSK_SKI1_1 | 294 | 298 | PF00082 | 0.271 |
CLV_PCSK_SKI1_1 | 571 | 575 | PF00082 | 0.569 |
DEG_SPOP_SBC_1 | 190 | 194 | PF00917 | 0.418 |
DEG_SPOP_SBC_1 | 304 | 308 | PF00917 | 0.373 |
DEG_SPOP_SBC_1 | 412 | 416 | PF00917 | 0.406 |
DOC_CKS1_1 | 441 | 446 | PF01111 | 0.449 |
DOC_CYCLIN_yCln2_LP_2 | 393 | 396 | PF00134 | 0.532 |
DOC_MAPK_MEF2A_6 | 267 | 276 | PF00069 | 0.467 |
DOC_PP1_RVXF_1 | 171 | 178 | PF00149 | 0.532 |
DOC_PP2B_LxvP_1 | 393 | 396 | PF13499 | 0.532 |
DOC_PP4_MxPP_1 | 473 | 476 | PF00568 | 0.373 |
DOC_USP7_MATH_1 | 191 | 195 | PF00917 | 0.464 |
DOC_USP7_MATH_1 | 304 | 308 | PF00917 | 0.418 |
DOC_USP7_MATH_1 | 315 | 319 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 412 | 416 | PF00917 | 0.418 |
DOC_USP7_MATH_1 | 591 | 595 | PF00917 | 0.767 |
DOC_USP7_MATH_1 | 688 | 692 | PF00917 | 0.564 |
DOC_USP7_UBL2_3 | 566 | 570 | PF12436 | 0.485 |
DOC_WW_Pin1_4 | 193 | 198 | PF00397 | 0.578 |
DOC_WW_Pin1_4 | 43 | 48 | PF00397 | 0.482 |
DOC_WW_Pin1_4 | 440 | 445 | PF00397 | 0.456 |
DOC_WW_Pin1_4 | 684 | 689 | PF00397 | 0.567 |
DOC_WW_Pin1_4 | 95 | 100 | PF00397 | 0.495 |
LIG_14-3-3_CanoR_1 | 141 | 145 | PF00244 | 0.595 |
LIG_eIF4E_1 | 256 | 262 | PF01652 | 0.532 |
LIG_FHA_1 | 128 | 134 | PF00498 | 0.373 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.507 |
LIG_FHA_2 | 166 | 172 | PF00498 | 0.435 |
LIG_FHA_2 | 306 | 312 | PF00498 | 0.405 |
LIG_FHA_2 | 32 | 38 | PF00498 | 0.647 |
LIG_FHA_2 | 466 | 472 | PF00498 | 0.533 |
LIG_FHA_2 | 483 | 489 | PF00498 | 0.518 |
LIG_FHA_2 | 517 | 523 | PF00498 | 0.434 |
LIG_LIR_Apic_2 | 37 | 41 | PF02991 | 0.579 |
LIG_LIR_Gen_1 | 468 | 478 | PF02991 | 0.494 |
LIG_LIR_Gen_1 | 579 | 589 | PF02991 | 0.583 |
LIG_LIR_Nem_3 | 579 | 584 | PF02991 | 0.576 |
LIG_LYPXL_SIV_4 | 99 | 107 | PF13949 | 0.317 |
LIG_NRBOX | 298 | 304 | PF00104 | 0.507 |
LIG_NRBOX | 429 | 435 | PF00104 | 0.467 |
LIG_NRBOX | 526 | 532 | PF00104 | 0.501 |
LIG_Pex14_2 | 262 | 266 | PF04695 | 0.549 |
LIG_PTAP_UEV_1 | 347 | 352 | PF05743 | 0.373 |
LIG_PTB_Apo_2 | 583 | 590 | PF02174 | 0.589 |
LIG_SH2_CRK | 205 | 209 | PF00017 | 0.467 |
LIG_SH2_CRK | 38 | 42 | PF00017 | 0.573 |
LIG_SH2_CRK | 462 | 466 | PF00017 | 0.467 |
LIG_SH2_NCK_1 | 38 | 42 | PF00017 | 0.641 |
LIG_SH2_PTP2 | 357 | 360 | PF00017 | 0.373 |
LIG_SH2_SRC | 100 | 103 | PF00017 | 0.317 |
LIG_SH2_SRC | 462 | 465 | PF00017 | 0.518 |
LIG_SH2_STAP1 | 462 | 466 | PF00017 | 0.532 |
LIG_SH2_STAT3 | 464 | 467 | PF00017 | 0.507 |
LIG_SH2_STAT5 | 100 | 103 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 357 | 360 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 38 | 41 | PF00017 | 0.572 |
LIG_SH2_STAT5 | 451 | 454 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 464 | 467 | PF00017 | 0.430 |
LIG_SH3_1 | 21 | 27 | PF00018 | 0.608 |
LIG_SH3_1 | 44 | 50 | PF00018 | 0.424 |
LIG_SH3_3 | 21 | 27 | PF00018 | 0.608 |
LIG_SH3_3 | 269 | 275 | PF00018 | 0.525 |
LIG_SH3_3 | 345 | 351 | PF00018 | 0.484 |
LIG_SH3_3 | 44 | 50 | PF00018 | 0.400 |
LIG_SH3_3 | 453 | 459 | PF00018 | 0.467 |
LIG_TRAF2_1 | 123 | 126 | PF00917 | 0.492 |
LIG_TRAF2_1 | 594 | 597 | PF00917 | 0.677 |
LIG_TYR_ITIM | 203 | 208 | PF00017 | 0.518 |
LIG_WW_3 | 394 | 398 | PF00397 | 0.525 |
MOD_CDC14_SPxK_1 | 196 | 199 | PF00782 | 0.409 |
MOD_CDK_SPK_2 | 440 | 445 | PF00069 | 0.373 |
MOD_CDK_SPK_2 | 684 | 689 | PF00069 | 0.504 |
MOD_CDK_SPxK_1 | 193 | 199 | PF00069 | 0.409 |
MOD_CK1_1 | 383 | 389 | PF00069 | 0.524 |
MOD_CK1_1 | 415 | 421 | PF00069 | 0.551 |
MOD_CK1_1 | 579 | 585 | PF00069 | 0.554 |
MOD_CK1_1 | 602 | 608 | PF00069 | 0.747 |
MOD_CK2_1 | 284 | 290 | PF00069 | 0.507 |
MOD_CK2_1 | 31 | 37 | PF00069 | 0.453 |
MOD_CK2_1 | 562 | 568 | PF00069 | 0.639 |
MOD_CK2_1 | 591 | 597 | PF00069 | 0.661 |
MOD_CK2_1 | 611 | 617 | PF00069 | 0.531 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.327 |
MOD_GlcNHglycan | 317 | 320 | PF01048 | 0.316 |
MOD_GlcNHglycan | 382 | 385 | PF01048 | 0.347 |
MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.344 |
MOD_GlcNHglycan | 418 | 421 | PF01048 | 0.376 |
MOD_GlcNHglycan | 488 | 492 | PF01048 | 0.382 |
MOD_GlcNHglycan | 602 | 605 | PF01048 | 0.703 |
MOD_GlcNHglycan | 613 | 616 | PF01048 | 0.658 |
MOD_GlcNHglycan | 655 | 658 | PF01048 | 0.796 |
MOD_GlcNHglycan | 666 | 669 | PF01048 | 0.752 |
MOD_GlcNHglycan | 675 | 678 | PF01048 | 0.550 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.399 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.588 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.474 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.558 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.532 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.544 |
MOD_GSK3_1 | 399 | 406 | PF00069 | 0.525 |
MOD_GSK3_1 | 407 | 414 | PF00069 | 0.549 |
MOD_GSK3_1 | 600 | 607 | PF00069 | 0.675 |
MOD_GSK3_1 | 684 | 691 | PF00069 | 0.677 |
MOD_N-GLC_1 | 246 | 251 | PF02516 | 0.332 |
MOD_N-GLC_1 | 30 | 35 | PF02516 | 0.649 |
MOD_N-GLC_1 | 576 | 581 | PF02516 | 0.547 |
MOD_N-GLC_1 | 684 | 689 | PF02516 | 0.617 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.533 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.590 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.532 |
MOD_NEK2_1 | 303 | 308 | PF00069 | 0.532 |
MOD_NEK2_1 | 329 | 334 | PF00069 | 0.478 |
MOD_NEK2_1 | 434 | 439 | PF00069 | 0.492 |
MOD_NEK2_1 | 658 | 663 | PF00069 | 0.646 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.676 |
MOD_PIKK_1 | 428 | 434 | PF00454 | 0.467 |
MOD_PIKK_1 | 639 | 645 | PF00454 | 0.513 |
MOD_PKA_2 | 140 | 146 | PF00069 | 0.600 |
MOD_PKA_2 | 156 | 162 | PF00069 | 0.385 |
MOD_PKA_2 | 17 | 23 | PF00069 | 0.599 |
MOD_PKA_2 | 591 | 597 | PF00069 | 0.677 |
MOD_PKA_2 | 688 | 694 | PF00069 | 0.749 |
MOD_Plk_1 | 482 | 488 | PF00069 | 0.498 |
MOD_Plk_1 | 579 | 585 | PF00069 | 0.554 |
MOD_Plk_2-3 | 284 | 290 | PF00069 | 0.494 |
MOD_Plk_4 | 140 | 146 | PF00069 | 0.578 |
MOD_Plk_4 | 465 | 471 | PF00069 | 0.506 |
MOD_ProDKin_1 | 193 | 199 | PF00069 | 0.578 |
MOD_ProDKin_1 | 43 | 49 | PF00069 | 0.475 |
MOD_ProDKin_1 | 440 | 446 | PF00069 | 0.456 |
MOD_ProDKin_1 | 684 | 690 | PF00069 | 0.567 |
MOD_ProDKin_1 | 95 | 101 | PF00069 | 0.486 |
MOD_SUMO_for_1 | 368 | 371 | PF00179 | 0.471 |
MOD_SUMO_rev_2 | 125 | 130 | PF00179 | 0.543 |
MOD_SUMO_rev_2 | 371 | 378 | PF00179 | 0.421 |
MOD_SUMO_rev_2 | 5 | 15 | PF00179 | 0.584 |
TRG_DiLeu_BaEn_1 | 140 | 145 | PF01217 | 0.507 |
TRG_DiLeu_BaLyEn_6 | 624 | 629 | PF01217 | 0.558 |
TRG_ENDOCYTIC_2 | 205 | 208 | PF00928 | 0.467 |
TRG_ENDOCYTIC_2 | 357 | 360 | PF00928 | 0.409 |
TRG_ENDOCYTIC_2 | 462 | 465 | PF00928 | 0.449 |
TRG_ENDOCYTIC_2 | 470 | 473 | PF00928 | 0.449 |
TRG_ER_diArg_1 | 120 | 122 | PF00400 | 0.532 |
TRG_ER_diArg_1 | 17 | 19 | PF00400 | 0.707 |
TRG_ER_diArg_1 | 545 | 547 | PF00400 | 0.374 |
TRG_Pf-PMV_PEXEL_1 | 110 | 114 | PF00026 | 0.292 |
TRG_Pf-PMV_PEXEL_1 | 297 | 301 | PF00026 | 0.307 |
TRG_Pf-PMV_PEXEL_1 | 445 | 449 | PF00026 | 0.283 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0E3 | Leptomonas seymouri | 55% | 87% |
A0A0S4JQM7 | Bodo saltans | 27% | 100% |
A0A1X0P9U8 | Trypanosomatidae | 31% | 88% |
A0A451EJS4 | Leishmania donovani | 84% | 98% |
A4H3N6 | Leishmania braziliensis | 64% | 100% |
A4HRW3 | Leishmania infantum | 84% | 98% |
C9ZKG8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 96% |
E9ACM0 | Leishmania major | 76% | 100% |