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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 11 |
GO:0043226 | organelle | 2 | 11 |
GO:0043227 | membrane-bounded organelle | 3 | 11 |
GO:0043229 | intracellular organelle | 3 | 11 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:0020023 | kinetoplast | 2 | 1 |
Related structures:
AlphaFold database: A0A3Q8IMS2
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 11 |
GO:0006259 | DNA metabolic process | 4 | 11 |
GO:0006281 | DNA repair | 5 | 11 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0006950 | response to stress | 2 | 11 |
GO:0006974 | DNA damage response | 4 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0033554 | cellular response to stress | 3 | 11 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 11 |
GO:0046483 | heterocycle metabolic process | 3 | 11 |
GO:0050896 | response to stimulus | 1 | 11 |
GO:0051716 | cellular response to stimulus | 2 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0090304 | nucleic acid metabolic process | 4 | 11 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 11 |
GO:0000012 | single strand break repair | 6 | 1 |
GO:0006302 | double-strand break repair | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004518 | nuclease activity | 4 | 11 |
GO:0008081 | phosphoric diester hydrolase activity | 5 | 11 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 11 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 11 |
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003677 | DNA binding | 4 | 1 |
GO:0003690 | double-stranded DNA binding | 5 | 1 |
GO:0003697 | single-stranded DNA binding | 5 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0017005 | 3'-tyrosyl-DNA phosphodiesterase activity | 5 | 1 |
GO:0070259 | tyrosyl-DNA phosphodiesterase activity | 4 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 1 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 100 | 104 | PF00656 | 0.373 |
CLV_C14_Caspase3-7 | 209 | 213 | PF00656 | 0.561 |
CLV_C14_Caspase3-7 | 366 | 370 | PF00656 | 0.412 |
CLV_NRD_NRD_1 | 186 | 188 | PF00675 | 0.247 |
CLV_NRD_NRD_1 | 320 | 322 | PF00675 | 0.259 |
CLV_NRD_NRD_1 | 512 | 514 | PF00675 | 0.323 |
CLV_NRD_NRD_1 | 675 | 677 | PF00675 | 0.673 |
CLV_NRD_NRD_1 | 98 | 100 | PF00675 | 0.294 |
CLV_PCSK_KEX2_1 | 320 | 322 | PF00082 | 0.259 |
CLV_PCSK_KEX2_1 | 428 | 430 | PF00082 | 0.297 |
CLV_PCSK_KEX2_1 | 677 | 679 | PF00082 | 0.576 |
CLV_PCSK_KEX2_1 | 98 | 100 | PF00082 | 0.294 |
CLV_PCSK_PC1ET2_1 | 428 | 430 | PF00082 | 0.349 |
CLV_PCSK_PC1ET2_1 | 677 | 679 | PF00082 | 0.587 |
CLV_PCSK_SKI1_1 | 161 | 165 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 200 | 204 | PF00082 | 0.297 |
CLV_PCSK_SKI1_1 | 321 | 325 | PF00082 | 0.327 |
CLV_PCSK_SKI1_1 | 42 | 46 | PF00082 | 0.304 |
CLV_PCSK_SKI1_1 | 428 | 432 | PF00082 | 0.228 |
CLV_PCSK_SKI1_1 | 494 | 498 | PF00082 | 0.318 |
CLV_PCSK_SKI1_1 | 565 | 569 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.207 |
CLV_Separin_Metazoa | 317 | 321 | PF03568 | 0.508 |
DEG_APCC_DBOX_1 | 140 | 148 | PF00400 | 0.459 |
DEG_APCC_DBOX_1 | 308 | 316 | PF00400 | 0.508 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.561 |
DEG_SCF_FBW7_1 | 589 | 596 | PF00400 | 0.459 |
DEG_SPOP_SBC_1 | 219 | 223 | PF00917 | 0.426 |
DOC_CDC14_PxL_1 | 72 | 80 | PF14671 | 0.444 |
DOC_CKS1_1 | 569 | 574 | PF01111 | 0.494 |
DOC_CYCLIN_yCln2_LP_2 | 147 | 153 | PF00134 | 0.436 |
DOC_CYCLIN_yCln2_LP_2 | 582 | 588 | PF00134 | 0.444 |
DOC_MAPK_gen_1 | 187 | 194 | PF00069 | 0.406 |
DOC_MAPK_gen_1 | 633 | 642 | PF00069 | 0.502 |
DOC_MAPK_MEF2A_6 | 395 | 404 | PF00069 | 0.444 |
DOC_MAPK_NFAT4_5 | 395 | 403 | PF00069 | 0.447 |
DOC_PP2B_LxvP_1 | 147 | 150 | PF13499 | 0.423 |
DOC_PP2B_LxvP_1 | 582 | 585 | PF13499 | 0.374 |
DOC_PP2B_LxvP_1 | 628 | 631 | PF13499 | 0.502 |
DOC_PP4_FxxP_1 | 431 | 434 | PF00568 | 0.412 |
DOC_PP4_FxxP_1 | 475 | 478 | PF00568 | 0.459 |
DOC_USP7_MATH_1 | 219 | 223 | PF00917 | 0.434 |
DOC_USP7_MATH_1 | 440 | 444 | PF00917 | 0.472 |
DOC_USP7_MATH_1 | 488 | 492 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 507 | 511 | PF00917 | 0.416 |
DOC_USP7_MATH_1 | 542 | 546 | PF00917 | 0.479 |
DOC_USP7_MATH_1 | 561 | 565 | PF00917 | 0.475 |
DOC_USP7_MATH_1 | 593 | 597 | PF00917 | 0.468 |
DOC_USP7_MATH_1 | 645 | 649 | PF00917 | 0.578 |
DOC_USP7_MATH_1 | 668 | 672 | PF00917 | 0.693 |
DOC_WW_Pin1_4 | 109 | 114 | PF00397 | 0.536 |
DOC_WW_Pin1_4 | 257 | 262 | PF00397 | 0.506 |
DOC_WW_Pin1_4 | 326 | 331 | PF00397 | 0.446 |
DOC_WW_Pin1_4 | 568 | 573 | PF00397 | 0.491 |
DOC_WW_Pin1_4 | 589 | 594 | PF00397 | 0.548 |
DOC_WW_Pin1_4 | 648 | 653 | PF00397 | 0.411 |
LIG_14-3-3_CanoR_1 | 130 | 139 | PF00244 | 0.389 |
LIG_14-3-3_CanoR_1 | 187 | 194 | PF00244 | 0.524 |
LIG_14-3-3_CanoR_1 | 320 | 326 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 388 | 392 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 395 | 401 | PF00244 | 0.486 |
LIG_Actin_WH2_2 | 159 | 174 | PF00022 | 0.459 |
LIG_BIR_III_4 | 636 | 640 | PF00653 | 0.401 |
LIG_BRCT_BRCA1_1 | 229 | 233 | PF00533 | 0.437 |
LIG_BRCT_BRCA1_1 | 544 | 548 | PF00533 | 0.526 |
LIG_BRCT_BRCA1_2 | 229 | 235 | PF00533 | 0.412 |
LIG_EH_1 | 118 | 122 | PF12763 | 0.508 |
LIG_eIF4E_1 | 583 | 589 | PF01652 | 0.545 |
LIG_EVH1_1 | 431 | 435 | PF00568 | 0.358 |
LIG_FHA_1 | 130 | 136 | PF00498 | 0.459 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.459 |
LIG_FHA_1 | 199 | 205 | PF00498 | 0.454 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.474 |
LIG_FHA_1 | 460 | 466 | PF00498 | 0.420 |
LIG_FHA_1 | 575 | 581 | PF00498 | 0.499 |
LIG_FHA_1 | 595 | 601 | PF00498 | 0.391 |
LIG_FHA_1 | 664 | 670 | PF00498 | 0.645 |
LIG_FHA_1 | 80 | 86 | PF00498 | 0.494 |
LIG_FHA_1 | 92 | 98 | PF00498 | 0.473 |
LIG_FHA_2 | 212 | 218 | PF00498 | 0.457 |
LIG_FHA_2 | 381 | 387 | PF00498 | 0.426 |
LIG_FHA_2 | 72 | 78 | PF00498 | 0.530 |
LIG_FHA_2 | 98 | 104 | PF00498 | 0.459 |
LIG_Integrin_isoDGR_2 | 167 | 169 | PF01839 | 0.173 |
LIG_LIR_Apic_2 | 472 | 478 | PF02991 | 0.373 |
LIG_LIR_Gen_1 | 22 | 32 | PF02991 | 0.486 |
LIG_LIR_Gen_1 | 482 | 488 | PF02991 | 0.413 |
LIG_LIR_Gen_1 | 54 | 64 | PF02991 | 0.413 |
LIG_LIR_Gen_1 | 545 | 556 | PF02991 | 0.533 |
LIG_LIR_Gen_1 | 620 | 628 | PF02991 | 0.322 |
LIG_LIR_Gen_1 | 643 | 654 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 22 | 27 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 482 | 486 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 54 | 59 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 545 | 551 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 620 | 624 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 643 | 649 | PF02991 | 0.422 |
LIG_Pex14_2 | 274 | 278 | PF04695 | 0.508 |
LIG_PTB_Apo_2 | 343 | 350 | PF02174 | 0.412 |
LIG_Rb_pABgroove_1 | 528 | 536 | PF01858 | 0.501 |
LIG_SH2_CRK | 483 | 487 | PF00017 | 0.432 |
LIG_SH2_CRK | 586 | 590 | PF00017 | 0.444 |
LIG_SH2_NCK_1 | 108 | 112 | PF00017 | 0.412 |
LIG_SH2_NCK_1 | 208 | 212 | PF00017 | 0.334 |
LIG_SH2_NCK_1 | 483 | 487 | PF00017 | 0.459 |
LIG_SH2_SRC | 299 | 302 | PF00017 | 0.412 |
LIG_SH2_STAP1 | 483 | 487 | PF00017 | 0.459 |
LIG_SH2_STAP1 | 594 | 598 | PF00017 | 0.398 |
LIG_SH2_STAT3 | 246 | 249 | PF00017 | 0.489 |
LIG_SH2_STAT3 | 339 | 342 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 108 | 111 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 193 | 196 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 246 | 249 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 583 | 586 | PF00017 | 0.534 |
LIG_SH2_STAT5 | 64 | 67 | PF00017 | 0.437 |
LIG_SH3_1 | 429 | 435 | PF00018 | 0.358 |
LIG_SH3_3 | 143 | 149 | PF00018 | 0.420 |
LIG_SH3_3 | 376 | 382 | PF00018 | 0.444 |
LIG_SH3_3 | 429 | 435 | PF00018 | 0.358 |
LIG_SH3_3 | 46 | 52 | PF00018 | 0.484 |
LIG_SUMO_SIM_anti_2 | 142 | 148 | PF11976 | 0.508 |
LIG_SUMO_SIM_par_1 | 84 | 89 | PF11976 | 0.480 |
LIG_TRAF2_1 | 382 | 385 | PF00917 | 0.550 |
LIG_TRAF2_1 | 420 | 423 | PF00917 | 0.389 |
LIG_TRAF2_1 | 613 | 616 | PF00917 | 0.445 |
LIG_TYR_ITIM | 584 | 589 | PF00017 | 0.451 |
LIG_WRC_WIRS_1 | 21 | 26 | PF05994 | 0.400 |
LIG_WW_2 | 149 | 152 | PF00397 | 0.469 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.484 |
MOD_CK1_1 | 221 | 227 | PF00069 | 0.562 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.528 |
MOD_CK1_1 | 322 | 328 | PF00069 | 0.459 |
MOD_CK1_1 | 329 | 335 | PF00069 | 0.425 |
MOD_CK1_1 | 341 | 347 | PF00069 | 0.441 |
MOD_CK1_1 | 543 | 549 | PF00069 | 0.428 |
MOD_CK1_1 | 63 | 69 | PF00069 | 0.484 |
MOD_CK1_1 | 648 | 654 | PF00069 | 0.410 |
MOD_CK1_1 | 79 | 85 | PF00069 | 0.508 |
MOD_CK2_1 | 211 | 217 | PF00069 | 0.376 |
MOD_CK2_1 | 380 | 386 | PF00069 | 0.426 |
MOD_CK2_1 | 417 | 423 | PF00069 | 0.420 |
MOD_CK2_1 | 551 | 557 | PF00069 | 0.519 |
MOD_CK2_1 | 71 | 77 | PF00069 | 0.516 |
MOD_CMANNOS | 391 | 394 | PF00535 | 0.259 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.342 |
MOD_GlcNHglycan | 209 | 212 | PF01048 | 0.270 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.339 |
MOD_GlcNHglycan | 283 | 287 | PF01048 | 0.239 |
MOD_GlcNHglycan | 321 | 324 | PF01048 | 0.297 |
MOD_GlcNHglycan | 360 | 363 | PF01048 | 0.275 |
MOD_GlcNHglycan | 366 | 369 | PF01048 | 0.286 |
MOD_GlcNHglycan | 499 | 502 | PF01048 | 0.220 |
MOD_GlcNHglycan | 537 | 540 | PF01048 | 0.288 |
MOD_GlcNHglycan | 542 | 545 | PF01048 | 0.271 |
MOD_GlcNHglycan | 77 | 81 | PF01048 | 0.248 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.179 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.478 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.518 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.476 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.492 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.365 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.419 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.454 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.452 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.362 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.476 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.429 |
MOD_GSK3_1 | 461 | 468 | PF00069 | 0.458 |
MOD_GSK3_1 | 497 | 504 | PF00069 | 0.420 |
MOD_GSK3_1 | 542 | 549 | PF00069 | 0.438 |
MOD_GSK3_1 | 589 | 596 | PF00069 | 0.518 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.462 |
MOD_GSK3_1 | 648 | 655 | PF00069 | 0.420 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.486 |
MOD_N-GLC_1 | 227 | 232 | PF02516 | 0.367 |
MOD_N-GLC_1 | 501 | 506 | PF02516 | 0.213 |
MOD_N-GLC_1 | 652 | 657 | PF02516 | 0.495 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.558 |
MOD_NEK2_1 | 171 | 176 | PF00069 | 0.459 |
MOD_NEK2_1 | 215 | 220 | PF00069 | 0.504 |
MOD_NEK2_1 | 291 | 296 | PF00069 | 0.463 |
MOD_NEK2_1 | 319 | 324 | PF00069 | 0.431 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.524 |
MOD_NEK2_1 | 349 | 354 | PF00069 | 0.505 |
MOD_NEK2_1 | 465 | 470 | PF00069 | 0.459 |
MOD_NEK2_1 | 496 | 501 | PF00069 | 0.445 |
MOD_NEK2_1 | 533 | 538 | PF00069 | 0.443 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.490 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.409 |
MOD_NEK2_1 | 97 | 102 | PF00069 | 0.563 |
MOD_NEK2_2 | 93 | 98 | PF00069 | 0.508 |
MOD_PIKK_1 | 186 | 192 | PF00454 | 0.428 |
MOD_PIKK_1 | 338 | 344 | PF00454 | 0.413 |
MOD_PIKK_1 | 501 | 507 | PF00454 | 0.463 |
MOD_PIKK_1 | 574 | 580 | PF00454 | 0.519 |
MOD_PKA_1 | 98 | 104 | PF00069 | 0.428 |
MOD_PKA_2 | 129 | 135 | PF00069 | 0.389 |
MOD_PKA_2 | 171 | 177 | PF00069 | 0.508 |
MOD_PKA_2 | 186 | 192 | PF00069 | 0.508 |
MOD_PKA_2 | 319 | 325 | PF00069 | 0.428 |
MOD_PKA_2 | 387 | 393 | PF00069 | 0.474 |
MOD_PKA_2 | 517 | 523 | PF00069 | 0.558 |
MOD_PKA_2 | 561 | 567 | PF00069 | 0.389 |
MOD_PKA_2 | 97 | 103 | PF00069 | 0.459 |
MOD_Plk_1 | 211 | 217 | PF00069 | 0.415 |
MOD_Plk_1 | 333 | 339 | PF00069 | 0.466 |
MOD_Plk_1 | 488 | 494 | PF00069 | 0.508 |
MOD_Plk_1 | 76 | 82 | PF00069 | 0.508 |
MOD_Plk_4 | 171 | 177 | PF00069 | 0.566 |
MOD_Plk_4 | 211 | 217 | PF00069 | 0.482 |
MOD_Plk_4 | 34 | 40 | PF00069 | 0.484 |
MOD_Plk_4 | 543 | 549 | PF00069 | 0.497 |
MOD_Plk_4 | 60 | 66 | PF00069 | 0.482 |
MOD_Plk_4 | 645 | 651 | PF00069 | 0.372 |
MOD_ProDKin_1 | 109 | 115 | PF00069 | 0.536 |
MOD_ProDKin_1 | 257 | 263 | PF00069 | 0.506 |
MOD_ProDKin_1 | 326 | 332 | PF00069 | 0.488 |
MOD_ProDKin_1 | 568 | 574 | PF00069 | 0.491 |
MOD_ProDKin_1 | 589 | 595 | PF00069 | 0.548 |
MOD_ProDKin_1 | 648 | 654 | PF00069 | 0.410 |
MOD_SUMO_rev_2 | 549 | 556 | PF00179 | 0.472 |
TRG_ENDOCYTIC_2 | 483 | 486 | PF00928 | 0.390 |
TRG_ENDOCYTIC_2 | 586 | 589 | PF00928 | 0.454 |
TRG_ER_diArg_1 | 319 | 321 | PF00400 | 0.459 |
TRG_ER_diArg_1 | 39 | 42 | PF00400 | 0.459 |
TRG_ER_diArg_1 | 659 | 662 | PF00400 | 0.529 |
TRG_ER_diArg_1 | 675 | 678 | PF00400 | 0.532 |
TRG_ER_diArg_1 | 97 | 99 | PF00400 | 0.494 |
TRG_NES_CRM1_1 | 77 | 91 | PF08389 | 0.508 |
TRG_NLS_MonoExtC_3 | 675 | 680 | PF00514 | 0.689 |
TRG_NLS_MonoExtN_4 | 675 | 680 | PF00514 | 0.700 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3C9 | Leptomonas seymouri | 50% | 98% |
A0A0S4JE96 | Bodo saltans | 30% | 97% |
A0A1X0NRE8 | Trypanosomatidae | 36% | 100% |
A0A3R7RCR4 | Trypanosoma rangeli | 32% | 100% |
A4HM15 | Leishmania braziliensis | 75% | 100% |
A4I9E7 | Leishmania infantum | 99% | 100% |
C9ZJR8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
E9B4E6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4Q3N1 | Leishmania major | 90% | 100% |
Q8H1D9 | Arabidopsis thaliana | 26% | 100% |
Q9VQM4 | Drosophila melanogaster | 23% | 100% |