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:0005634 | nucleus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9ATW1
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 10 |
GO:0006259 | DNA metabolic process | 4 | 10 |
GO:0006281 | DNA repair | 5 | 10 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
GO:0006950 | response to stress | 2 | 10 |
GO:0006974 | DNA damage response | 4 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0033554 | cellular response to stress | 3 | 10 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 10 |
GO:0043170 | macromolecule metabolic process | 3 | 10 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0044238 | primary metabolic process | 2 | 10 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 10 |
GO:0046483 | heterocycle metabolic process | 3 | 10 |
GO:0050896 | response to stimulus | 1 | 10 |
GO:0051716 | cellular response to stimulus | 2 | 10 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
GO:0090304 | nucleic acid metabolic process | 4 | 10 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 10 |
GO:0006284 | base-excision repair | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 10 |
GO:0003677 | DNA binding | 4 | 10 |
GO:0003824 | catalytic activity | 1 | 10 |
GO:0004518 | nuclease activity | 4 | 10 |
GO:0004519 | endonuclease activity | 5 | 10 |
GO:0004527 | exonuclease activity | 5 | 7 |
GO:0005488 | binding | 1 | 10 |
GO:0016787 | hydrolase activity | 2 | 10 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
GO:0003906 | DNA-(apurinic or apyrimidinic site) endonuclease activity | 4 | 3 |
GO:0004529 | DNA exonuclease activity | 5 | 1 |
GO:0004536 | DNA nuclease activity | 4 | 1 |
GO:0008081 | phosphoric diester hydrolase activity | 5 | 1 |
GO:0008296 | 3'-5'-DNA exonuclease activity | 7 | 1 |
GO:0008309 | double-stranded DNA exodeoxyribonuclease activity | 7 | 1 |
GO:0008311 | double-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:0042578 | phosphoric ester hydrolase activity | 4 | 1 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 3 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 3 |
GO:0016829 | lyase activity | 2 | 2 |
GO:0016835 | carbon-oxygen lyase activity | 3 | 2 |
GO:0140078 | class I DNA-(apurinic or apyrimidinic site) endonuclease activity | 4 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 108 | 112 | PF00656 | 0.245 |
CLV_C14_Caspase3-7 | 441 | 445 | PF00656 | 0.336 |
CLV_NRD_NRD_1 | 134 | 136 | PF00675 | 0.298 |
CLV_NRD_NRD_1 | 227 | 229 | PF00675 | 0.297 |
CLV_NRD_NRD_1 | 486 | 488 | PF00675 | 0.333 |
CLV_NRD_NRD_1 | 65 | 67 | PF00675 | 0.391 |
CLV_NRD_NRD_1 | 82 | 84 | PF00675 | 0.391 |
CLV_PCSK_FUR_1 | 484 | 488 | PF00082 | 0.298 |
CLV_PCSK_KEX2_1 | 227 | 229 | PF00082 | 0.274 |
CLV_PCSK_KEX2_1 | 262 | 264 | PF00082 | 0.460 |
CLV_PCSK_KEX2_1 | 486 | 488 | PF00082 | 0.274 |
CLV_PCSK_KEX2_1 | 65 | 67 | PF00082 | 0.391 |
CLV_PCSK_KEX2_1 | 686 | 688 | PF00082 | 0.730 |
CLV_PCSK_KEX2_1 | 80 | 82 | PF00082 | 0.391 |
CLV_PCSK_PC1ET2_1 | 262 | 264 | PF00082 | 0.336 |
CLV_PCSK_PC1ET2_1 | 686 | 688 | PF00082 | 0.730 |
CLV_PCSK_PC1ET2_1 | 80 | 82 | PF00082 | 0.282 |
CLV_PCSK_SKI1_1 | 136 | 140 | PF00082 | 0.284 |
CLV_PCSK_SKI1_1 | 313 | 317 | PF00082 | 0.371 |
CLV_PCSK_SKI1_1 | 653 | 657 | PF00082 | 0.401 |
DEG_APCC_DBOX_1 | 227 | 235 | PF00400 | 0.298 |
DEG_APCC_DBOX_1 | 312 | 320 | PF00400 | 0.336 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.296 |
DEG_SPOP_SBC_1 | 289 | 293 | PF00917 | 0.302 |
DEG_SPOP_SBC_1 | 402 | 406 | PF00917 | 0.302 |
DOC_CKS1_1 | 595 | 600 | PF01111 | 0.344 |
DOC_CYCLIN_yCln2_LP_2 | 322 | 325 | PF00134 | 0.336 |
DOC_MAPK_MEF2A_6 | 395 | 403 | PF00069 | 0.394 |
DOC_MAPK_MEF2A_6 | 634 | 643 | PF00069 | 0.515 |
DOC_PP1_RVXF_1 | 134 | 141 | PF00149 | 0.298 |
DOC_PP1_RVXF_1 | 183 | 189 | PF00149 | 0.407 |
DOC_PP1_RVXF_1 | 580 | 587 | PF00149 | 0.402 |
DOC_PP2B_LxvP_1 | 322 | 325 | PF13499 | 0.336 |
DOC_PP2B_LxvP_1 | 399 | 402 | PF13499 | 0.383 |
DOC_PP2B_PxIxI_1 | 205 | 211 | PF00149 | 0.391 |
DOC_PP4_FxxP_1 | 595 | 598 | PF00568 | 0.337 |
DOC_USP7_MATH_1 | 289 | 293 | PF00917 | 0.385 |
DOC_USP7_MATH_1 | 325 | 329 | PF00917 | 0.428 |
DOC_USP7_MATH_1 | 356 | 360 | PF00917 | 0.302 |
DOC_USP7_MATH_1 | 368 | 372 | PF00917 | 0.184 |
DOC_USP7_MATH_1 | 402 | 406 | PF00917 | 0.302 |
DOC_USP7_MATH_1 | 533 | 537 | PF00917 | 0.583 |
DOC_USP7_MATH_1 | 655 | 659 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 660 | 664 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.386 |
DOC_USP7_UBL2_3 | 258 | 262 | PF12436 | 0.481 |
DOC_WW_Pin1_4 | 362 | 367 | PF00397 | 0.485 |
DOC_WW_Pin1_4 | 450 | 455 | PF00397 | 0.480 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.391 |
DOC_WW_Pin1_4 | 594 | 599 | PF00397 | 0.340 |
LIG_14-3-3_CanoR_1 | 135 | 141 | PF00244 | 0.298 |
LIG_14-3-3_CanoR_1 | 157 | 167 | PF00244 | 0.298 |
LIG_14-3-3_CanoR_1 | 181 | 185 | PF00244 | 0.262 |
LIG_14-3-3_CanoR_1 | 354 | 362 | PF00244 | 0.406 |
LIG_14-3-3_CanoR_1 | 400 | 409 | PF00244 | 0.403 |
LIG_14-3-3_CanoR_1 | 411 | 420 | PF00244 | 0.336 |
LIG_14-3-3_CanoR_1 | 525 | 533 | PF00244 | 0.599 |
LIG_APCC_ABBA_1 | 382 | 387 | PF00400 | 0.298 |
LIG_BRCT_BRCA1_1 | 143 | 147 | PF00533 | 0.315 |
LIG_BRCT_BRCA1_1 | 388 | 392 | PF00533 | 0.298 |
LIG_BRCT_BRCA1_1 | 527 | 531 | PF00533 | 0.463 |
LIG_CtBP_PxDLS_1 | 342 | 346 | PF00389 | 0.336 |
LIG_CtBP_PxDLS_1 | 53 | 57 | PF00389 | 0.374 |
LIG_deltaCOP1_diTrp_1 | 111 | 117 | PF00928 | 0.277 |
LIG_EVH1_1 | 564 | 568 | PF00568 | 0.519 |
LIG_EVH1_2 | 565 | 569 | PF00568 | 0.543 |
LIG_FHA_1 | 181 | 187 | PF00498 | 0.317 |
LIG_FHA_1 | 248 | 254 | PF00498 | 0.310 |
LIG_FHA_1 | 293 | 299 | PF00498 | 0.454 |
LIG_FHA_1 | 433 | 439 | PF00498 | 0.380 |
LIG_FHA_1 | 654 | 660 | PF00498 | 0.513 |
LIG_FHA_2 | 30 | 36 | PF00498 | 0.282 |
LIG_FHA_2 | 476 | 482 | PF00498 | 0.274 |
LIG_FHA_2 | 491 | 497 | PF00498 | 0.274 |
LIG_FHA_2 | 616 | 622 | PF00498 | 0.505 |
LIG_GBD_Chelix_1 | 264 | 272 | PF00786 | 0.302 |
LIG_Integrin_RGD_1 | 723 | 725 | PF01839 | 0.497 |
LIG_LIR_Apic_2 | 592 | 598 | PF02991 | 0.334 |
LIG_LIR_Gen_1 | 111 | 119 | PF02991 | 0.298 |
LIG_LIR_Gen_1 | 371 | 382 | PF02991 | 0.336 |
LIG_LIR_Gen_1 | 496 | 505 | PF02991 | 0.274 |
LIG_LIR_Gen_1 | 540 | 551 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 111 | 116 | PF02991 | 0.277 |
LIG_LIR_Nem_3 | 20 | 25 | PF02991 | 0.274 |
LIG_LIR_Nem_3 | 371 | 377 | PF02991 | 0.322 |
LIG_LIR_Nem_3 | 496 | 500 | PF02991 | 0.274 |
LIG_LIR_Nem_3 | 540 | 546 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 583 | 589 | PF02991 | 0.449 |
LIG_MYND_1 | 467 | 471 | PF01753 | 0.391 |
LIG_NRBOX | 230 | 236 | PF00104 | 0.391 |
LIG_OCRL_FandH_1 | 21 | 33 | PF00620 | 0.313 |
LIG_PCNA_yPIPBox_3 | 363 | 377 | PF02747 | 0.333 |
LIG_PDZ_Class_3 | 731 | 736 | PF00595 | 0.583 |
LIG_Pex14_2 | 184 | 188 | PF04695 | 0.298 |
LIG_Pex14_2 | 2 | 6 | PF04695 | 0.313 |
LIG_PTB_Apo_2 | 558 | 565 | PF02174 | 0.508 |
LIG_PTB_Phospho_1 | 558 | 564 | PF10480 | 0.505 |
LIG_Rb_pABgroove_1 | 343 | 351 | PF01858 | 0.336 |
LIG_SH2_CRK | 374 | 378 | PF00017 | 0.332 |
LIG_SH2_CRK | 637 | 641 | PF00017 | 0.410 |
LIG_SH2_NCK_1 | 338 | 342 | PF00017 | 0.391 |
LIG_SH2_PTP2 | 497 | 500 | PF00017 | 0.274 |
LIG_SH2_STAP1 | 357 | 361 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 172 | 175 | PF00017 | 0.307 |
LIG_SH2_STAT5 | 217 | 220 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 357 | 360 | PF00017 | 0.257 |
LIG_SH2_STAT5 | 472 | 475 | PF00017 | 0.291 |
LIG_SH2_STAT5 | 477 | 480 | PF00017 | 0.257 |
LIG_SH2_STAT5 | 497 | 500 | PF00017 | 0.274 |
LIG_SH3_1 | 468 | 474 | PF00018 | 0.336 |
LIG_SH3_3 | 168 | 174 | PF00018 | 0.391 |
LIG_SH3_3 | 461 | 467 | PF00018 | 0.328 |
LIG_SH3_3 | 468 | 474 | PF00018 | 0.279 |
LIG_SH3_3 | 562 | 568 | PF00018 | 0.429 |
LIG_SH3_3 | 593 | 599 | PF00018 | 0.376 |
LIG_SH3_3 | 65 | 71 | PF00018 | 0.462 |
LIG_SH3_3 | 656 | 662 | PF00018 | 0.653 |
LIG_SH3_4 | 661 | 668 | PF00018 | 0.482 |
LIG_SUMO_SIM_anti_2 | 457 | 463 | PF11976 | 0.423 |
LIG_SUMO_SIM_par_1 | 206 | 212 | PF11976 | 0.298 |
LIG_SUMO_SIM_par_1 | 295 | 303 | PF11976 | 0.349 |
LIG_SUMO_SIM_par_1 | 729 | 735 | PF11976 | 0.619 |
LIG_TRAF2_2 | 598 | 603 | PF00917 | 0.346 |
LIG_TYR_ITIM | 495 | 500 | PF00017 | 0.274 |
LIG_UBA3_1 | 36 | 43 | PF00899 | 0.391 |
LIG_WRC_WIRS_1 | 130 | 135 | PF05994 | 0.325 |
LIG_WRC_WIRS_1 | 643 | 648 | PF05994 | 0.515 |
LIG_WRC_WIRS_1 | 695 | 700 | PF05994 | 0.574 |
LIG_WW_3 | 323 | 327 | PF00397 | 0.336 |
MOD_CK1_1 | 115 | 121 | PF00069 | 0.337 |
MOD_CK1_1 | 12 | 18 | PF00069 | 0.333 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.333 |
MOD_CK1_1 | 282 | 288 | PF00069 | 0.410 |
MOD_CK1_1 | 292 | 298 | PF00069 | 0.375 |
MOD_CK1_1 | 299 | 305 | PF00069 | 0.426 |
MOD_CK1_1 | 307 | 313 | PF00069 | 0.466 |
MOD_CK1_1 | 386 | 392 | PF00069 | 0.403 |
MOD_CK1_1 | 691 | 697 | PF00069 | 0.708 |
MOD_CK1_1 | 93 | 99 | PF00069 | 0.395 |
MOD_CK2_1 | 145 | 151 | PF00069 | 0.240 |
MOD_CK2_1 | 615 | 621 | PF00069 | 0.501 |
MOD_CK2_1 | 710 | 716 | PF00069 | 0.670 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.298 |
MOD_GlcNHglycan | 284 | 287 | PF01048 | 0.391 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.412 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.395 |
MOD_GlcNHglycan | 387 | 391 | PF01048 | 0.391 |
MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.444 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.476 |
MOD_GlcNHglycan | 501 | 504 | PF01048 | 0.343 |
MOD_GlcNHglycan | 527 | 530 | PF01048 | 0.609 |
MOD_GlcNHglycan | 625 | 628 | PF01048 | 0.622 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.258 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.292 |
MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.305 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.366 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.363 |
MOD_GSK3_1 | 299 | 306 | PF00069 | 0.389 |
MOD_GSK3_1 | 432 | 439 | PF00069 | 0.430 |
MOD_GSK3_1 | 649 | 656 | PF00069 | 0.442 |
MOD_GSK3_1 | 693 | 700 | PF00069 | 0.745 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.395 |
MOD_N-GLC_1 | 213 | 218 | PF02516 | 0.274 |
MOD_N-GLC_1 | 304 | 309 | PF02516 | 0.330 |
MOD_N-GLC_1 | 525 | 530 | PF02516 | 0.437 |
MOD_N-GLC_1 | 698 | 703 | PF02516 | 0.547 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.291 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.280 |
MOD_NEK2_1 | 361 | 366 | PF00069 | 0.368 |
MOD_NEK2_1 | 432 | 437 | PF00069 | 0.316 |
MOD_NEK2_1 | 499 | 504 | PF00069 | 0.336 |
MOD_NEK2_1 | 527 | 532 | PF00069 | 0.442 |
MOD_NEK2_1 | 546 | 551 | PF00069 | 0.271 |
MOD_NEK2_1 | 569 | 574 | PF00069 | 0.448 |
MOD_NEK2_1 | 623 | 628 | PF00069 | 0.543 |
MOD_NEK2_1 | 698 | 703 | PF00069 | 0.729 |
MOD_NEK2_2 | 180 | 185 | PF00069 | 0.245 |
MOD_NEK2_2 | 222 | 227 | PF00069 | 0.333 |
MOD_NEK2_2 | 642 | 647 | PF00069 | 0.599 |
MOD_OFUCOSY | 473 | 479 | PF10250 | 0.335 |
MOD_PIKK_1 | 12 | 18 | PF00454 | 0.370 |
MOD_PIKK_1 | 141 | 147 | PF00454 | 0.329 |
MOD_PKA_1 | 653 | 659 | PF00069 | 0.460 |
MOD_PKA_1 | 82 | 88 | PF00069 | 0.211 |
MOD_PKA_2 | 18 | 24 | PF00069 | 0.328 |
MOD_PKA_2 | 180 | 186 | PF00069 | 0.282 |
MOD_PKA_2 | 325 | 331 | PF00069 | 0.455 |
MOD_PKA_2 | 82 | 88 | PF00069 | 0.344 |
MOD_Plk_1 | 213 | 219 | PF00069 | 0.274 |
MOD_Plk_1 | 307 | 313 | PF00069 | 0.268 |
MOD_Plk_4 | 112 | 118 | PF00069 | 0.314 |
MOD_Plk_4 | 230 | 236 | PF00069 | 0.280 |
MOD_Plk_4 | 432 | 438 | PF00069 | 0.333 |
MOD_Plk_4 | 642 | 648 | PF00069 | 0.515 |
MOD_ProDKin_1 | 362 | 368 | PF00069 | 0.485 |
MOD_ProDKin_1 | 450 | 456 | PF00069 | 0.480 |
MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.391 |
MOD_ProDKin_1 | 594 | 600 | PF00069 | 0.344 |
MOD_SUMO_rev_2 | 35 | 45 | PF00179 | 0.274 |
MOD_SUMO_rev_2 | 626 | 636 | PF00179 | 0.526 |
TRG_AP2beta_CARGO_1 | 540 | 550 | PF09066 | 0.443 |
TRG_DiLeu_BaLyEn_6 | 392 | 397 | PF01217 | 0.391 |
TRG_DiLeu_BaLyEn_6 | 451 | 456 | PF01217 | 0.336 |
TRG_ENDOCYTIC_2 | 374 | 377 | PF00928 | 0.332 |
TRG_ENDOCYTIC_2 | 497 | 500 | PF00928 | 0.274 |
TRG_ER_diArg_1 | 226 | 228 | PF00400 | 0.275 |
TRG_ER_diArg_1 | 429 | 432 | PF00400 | 0.268 |
TRG_ER_diArg_1 | 466 | 469 | PF00400 | 0.468 |
TRG_ER_diArg_1 | 484 | 487 | PF00400 | 0.231 |
TRG_ER_diArg_1 | 65 | 67 | PF00400 | 0.391 |
TRG_ER_diArg_1 | 81 | 83 | PF00400 | 0.391 |
TRG_NLS_Bipartite_1 | 65 | 84 | PF00514 | 0.177 |
TRG_NLS_MonoCore_2 | 79 | 84 | PF00514 | 0.177 |
TRG_Pf-PMV_PEXEL_1 | 346 | 350 | PF00026 | 0.391 |
TRG_Pf-PMV_PEXEL_1 | 486 | 491 | PF00026 | 0.336 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PB73 | Leptomonas seymouri | 58% | 99% |
A0A1X0P3V4 | Trypanosomatidae | 36% | 100% |
A0A3R7M024 | Trypanosoma rangeli | 41% | 100% |
A0A3S7XBT9 | Leishmania donovani | 89% | 100% |
A4IDU8 | Leishmania infantum | 89% | 100% |
D0A8S3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
E9AIY2 | Leishmania braziliensis | 80% | 100% |
Q4Q0N5 | Leishmania major | 90% | 100% |