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: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005694 | chromosome | 5 | 6 |
GO:0043226 | organelle | 2 | 6 |
GO:0043228 | non-membrane-bounded organelle | 3 | 6 |
GO:0043229 | intracellular organelle | 3 | 6 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
GO:0000228 | nuclear chromosome | 6 | 1 |
Related structures:
AlphaFold database: A4H8I5
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 6 |
GO:0006259 | DNA metabolic process | 4 | 6 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 6 |
GO:0006807 | nitrogen compound metabolic process | 2 | 6 |
GO:0008152 | metabolic process | 1 | 6 |
GO:0009987 | cellular process | 1 | 6 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 6 |
GO:0043170 | macromolecule metabolic process | 3 | 6 |
GO:0044237 | cellular metabolic process | 2 | 6 |
GO:0044238 | primary metabolic process | 2 | 6 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 6 |
GO:0046483 | heterocycle metabolic process | 3 | 6 |
GO:0071704 | organic substance metabolic process | 2 | 6 |
GO:0090304 | nucleic acid metabolic process | 4 | 6 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 6 |
GO:0000706 | meiotic DNA double-strand break processing | 3 | 1 |
GO:0000729 | DNA double-strand break processing | 5 | 1 |
GO:0006310 | DNA recombination | 5 | 1 |
GO:0007131 | reciprocal meiotic recombination | 3 | 1 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0022414 | reproductive process | 1 | 1 |
GO:0035825 | homologous recombination | 6 | 1 |
GO:0042138 | meiotic DNA double-strand break formation | 4 | 1 |
GO:0061982 | meiosis I cell cycle process | 3 | 1 |
GO:0090305 | nucleic acid phosphodiester bond hydrolysis | 5 | 1 |
GO:0140527 | reciprocal homologous recombination | 7 | 1 |
GO:1903046 | meiotic cell cycle process | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 6 |
GO:0003676 | nucleic acid binding | 3 | 6 |
GO:0003677 | DNA binding | 4 | 6 |
GO:0003824 | catalytic activity | 1 | 6 |
GO:0003916 | DNA topoisomerase activity | 3 | 6 |
GO:0003918 | DNA topoisomerase type II (double strand cut, ATP-hydrolyzing) activity | 3 | 6 |
GO:0005488 | binding | 1 | 6 |
GO:0005524 | ATP binding | 5 | 6 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 6 |
GO:0016853 | isomerase activity | 2 | 6 |
GO:0017076 | purine nucleotide binding | 4 | 6 |
GO:0030554 | adenyl nucleotide binding | 5 | 6 |
GO:0032553 | ribonucleotide binding | 3 | 6 |
GO:0032555 | purine ribonucleotide binding | 4 | 6 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 6 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 6 |
GO:0036094 | small molecule binding | 2 | 6 |
GO:0043167 | ion binding | 2 | 6 |
GO:0043168 | anion binding | 3 | 6 |
GO:0043169 | cation binding | 3 | 6 |
GO:0046872 | metal ion binding | 4 | 6 |
GO:0097159 | organic cyclic compound binding | 2 | 6 |
GO:0097367 | carbohydrate derivative binding | 2 | 6 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 6 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 6 |
GO:0140657 | ATP-dependent activity | 1 | 6 |
GO:1901265 | nucleoside phosphate binding | 3 | 6 |
GO:1901363 | heterocyclic compound binding | 2 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 290 | 294 | PF00656 | 0.479 |
CLV_C14_Caspase3-7 | 381 | 385 | PF00656 | 0.414 |
CLV_C14_Caspase3-7 | 420 | 424 | PF00656 | 0.556 |
CLV_C14_Caspase3-7 | 502 | 506 | PF00656 | 0.436 |
CLV_NRD_NRD_1 | 27 | 29 | PF00675 | 0.357 |
CLV_NRD_NRD_1 | 503 | 505 | PF00675 | 0.454 |
CLV_NRD_NRD_1 | 599 | 601 | PF00675 | 0.346 |
CLV_NRD_NRD_1 | 629 | 631 | PF00675 | 0.612 |
CLV_NRD_NRD_1 | 649 | 651 | PF00675 | 0.269 |
CLV_NRD_NRD_1 | 67 | 69 | PF00675 | 0.607 |
CLV_NRD_NRD_1 | 83 | 85 | PF00675 | 0.508 |
CLV_PCSK_KEX2_1 | 27 | 29 | PF00082 | 0.357 |
CLV_PCSK_KEX2_1 | 503 | 505 | PF00082 | 0.465 |
CLV_PCSK_KEX2_1 | 554 | 556 | PF00082 | 0.703 |
CLV_PCSK_KEX2_1 | 599 | 601 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 629 | 631 | PF00082 | 0.606 |
CLV_PCSK_KEX2_1 | 649 | 651 | PF00082 | 0.389 |
CLV_PCSK_KEX2_1 | 67 | 69 | PF00082 | 0.613 |
CLV_PCSK_KEX2_1 | 83 | 85 | PF00082 | 0.605 |
CLV_PCSK_PC1ET2_1 | 554 | 556 | PF00082 | 0.677 |
CLV_PCSK_PC7_1 | 550 | 556 | PF00082 | 0.510 |
CLV_PCSK_PC7_1 | 595 | 601 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 174 | 178 | PF00082 | 0.227 |
CLV_PCSK_SKI1_1 | 284 | 288 | PF00082 | 0.586 |
CLV_PCSK_SKI1_1 | 345 | 349 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 378 | 382 | PF00082 | 0.325 |
CLV_PCSK_SKI1_1 | 600 | 604 | PF00082 | 0.301 |
DEG_APCC_DBOX_1 | 133 | 141 | PF00400 | 0.293 |
DEG_APCC_DBOX_1 | 321 | 329 | PF00400 | 0.351 |
DEG_APCC_DBOX_1 | 344 | 352 | PF00400 | 0.421 |
DOC_ANK_TNKS_1 | 356 | 363 | PF00023 | 0.292 |
DOC_CDC14_PxL_1 | 397 | 405 | PF14671 | 0.418 |
DOC_CYCLIN_yCln2_LP_2 | 258 | 264 | PF00134 | 0.491 |
DOC_MAPK_gen_1 | 132 | 140 | PF00069 | 0.307 |
DOC_MAPK_gen_1 | 184 | 192 | PF00069 | 0.293 |
DOC_MAPK_gen_1 | 27 | 33 | PF00069 | 0.360 |
DOC_MAPK_gen_1 | 554 | 563 | PF00069 | 0.570 |
DOC_MAPK_MEF2A_6 | 134 | 142 | PF00069 | 0.318 |
DOC_MAPK_MEF2A_6 | 327 | 334 | PF00069 | 0.341 |
DOC_MAPK_MEF2A_6 | 554 | 563 | PF00069 | 0.495 |
DOC_PP2B_LxvP_1 | 183 | 186 | PF13499 | 0.293 |
DOC_PP2B_LxvP_1 | 41 | 44 | PF13499 | 0.480 |
DOC_USP7_MATH_1 | 123 | 127 | PF00917 | 0.568 |
DOC_USP7_MATH_1 | 270 | 274 | PF00917 | 0.536 |
DOC_USP7_MATH_1 | 380 | 384 | PF00917 | 0.510 |
DOC_USP7_MATH_1 | 411 | 415 | PF00917 | 0.329 |
DOC_USP7_MATH_1 | 468 | 472 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 491 | 495 | PF00917 | 0.645 |
DOC_USP7_MATH_1 | 634 | 638 | PF00917 | 0.426 |
DOC_WW_Pin1_4 | 257 | 262 | PF00397 | 0.526 |
DOC_WW_Pin1_4 | 266 | 271 | PF00397 | 0.479 |
DOC_WW_Pin1_4 | 299 | 304 | PF00397 | 0.299 |
DOC_WW_Pin1_4 | 439 | 444 | PF00397 | 0.794 |
DOC_WW_Pin1_4 | 487 | 492 | PF00397 | 0.567 |
DOC_WW_Pin1_4 | 522 | 527 | PF00397 | 0.572 |
DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.444 |
LIG_14-3-3_CanoR_1 | 207 | 212 | PF00244 | 0.375 |
LIG_14-3-3_CanoR_1 | 378 | 386 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 558 | 562 | PF00244 | 0.534 |
LIG_14-3-3_CanoR_1 | 572 | 576 | PF00244 | 0.530 |
LIG_14-3-3_CanoR_1 | 584 | 588 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 599 | 603 | PF00244 | 0.508 |
LIG_14-3-3_CanoR_1 | 67 | 75 | PF00244 | 0.533 |
LIG_BRCT_BRCA1_1 | 335 | 339 | PF00533 | 0.283 |
LIG_BRCT_BRCA1_1 | 614 | 618 | PF00533 | 0.338 |
LIG_CSL_BTD_1 | 41 | 44 | PF09270 | 0.359 |
LIG_eIF4E_1 | 342 | 348 | PF01652 | 0.355 |
LIG_FHA_1 | 166 | 172 | PF00498 | 0.348 |
LIG_FHA_1 | 229 | 235 | PF00498 | 0.359 |
LIG_FHA_1 | 408 | 414 | PF00498 | 0.396 |
LIG_FHA_1 | 508 | 514 | PF00498 | 0.322 |
LIG_FHA_1 | 51 | 57 | PF00498 | 0.486 |
LIG_FHA_2 | 152 | 158 | PF00498 | 0.293 |
LIG_FHA_2 | 2 | 8 | PF00498 | 0.375 |
LIG_FHA_2 | 242 | 248 | PF00498 | 0.494 |
LIG_FHA_2 | 379 | 385 | PF00498 | 0.448 |
LIG_FHA_2 | 418 | 424 | PF00498 | 0.492 |
LIG_FHA_2 | 500 | 506 | PF00498 | 0.413 |
LIG_FHA_2 | 533 | 539 | PF00498 | 0.542 |
LIG_FHA_2 | 80 | 86 | PF00498 | 0.580 |
LIG_Integrin_RGD_1 | 149 | 151 | PF01839 | 0.312 |
LIG_LIR_Apic_2 | 607 | 613 | PF02991 | 0.456 |
LIG_LIR_Gen_1 | 157 | 167 | PF02991 | 0.348 |
LIG_LIR_Gen_1 | 2 | 13 | PF02991 | 0.446 |
LIG_LIR_Gen_1 | 251 | 262 | PF02991 | 0.636 |
LIG_LIR_LC3C_4 | 230 | 235 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 141 | 147 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 157 | 163 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 2 | 8 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 205 | 209 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 251 | 257 | PF02991 | 0.640 |
LIG_LIR_Nem_3 | 336 | 342 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 39 | 45 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 394 | 400 | PF02991 | 0.449 |
LIG_MYND_1 | 326 | 330 | PF01753 | 0.348 |
LIG_NRBOX | 36 | 42 | PF00104 | 0.443 |
LIG_NRBOX | 515 | 521 | PF00104 | 0.456 |
LIG_SH2_CRK | 160 | 164 | PF00017 | 0.293 |
LIG_SH2_CRK | 206 | 210 | PF00017 | 0.395 |
LIG_SH2_CRK | 570 | 574 | PF00017 | 0.443 |
LIG_SH2_CRK | 610 | 614 | PF00017 | 0.476 |
LIG_SH2_NCK_1 | 441 | 445 | PF00017 | 0.557 |
LIG_SH2_NCK_1 | 610 | 614 | PF00017 | 0.476 |
LIG_SH2_PTP2 | 398 | 401 | PF00017 | 0.308 |
LIG_SH2_SRC | 478 | 481 | PF00017 | 0.516 |
LIG_SH2_STAP1 | 614 | 618 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 199 | 202 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 32 | 35 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 398 | 401 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 441 | 444 | PF00017 | 0.526 |
LIG_SH2_STAT5 | 610 | 613 | PF00017 | 0.458 |
LIG_SH3_3 | 112 | 118 | PF00018 | 0.526 |
LIG_SH3_3 | 353 | 359 | PF00018 | 0.312 |
LIG_SH3_3 | 545 | 551 | PF00018 | 0.525 |
LIG_SH3_3 | 91 | 97 | PF00018 | 0.644 |
LIG_SUMO_SIM_par_1 | 11 | 17 | PF11976 | 0.470 |
LIG_SUMO_SIM_par_1 | 136 | 141 | PF11976 | 0.348 |
LIG_SUMO_SIM_par_1 | 230 | 239 | PF11976 | 0.319 |
LIG_SUMO_SIM_par_1 | 307 | 312 | PF11976 | 0.307 |
LIG_SUMO_SIM_par_1 | 92 | 100 | PF11976 | 0.527 |
LIG_TRAF2_1 | 219 | 222 | PF00917 | 0.497 |
LIG_TRAF2_1 | 236 | 239 | PF00917 | 0.317 |
LIG_TRAF2_1 | 97 | 100 | PF00917 | 0.524 |
LIG_TYR_ITIM | 158 | 163 | PF00017 | 0.348 |
LIG_TYR_ITIM | 204 | 209 | PF00017 | 0.371 |
LIG_UBA3_1 | 40 | 46 | PF00899 | 0.463 |
MOD_CK1_1 | 260 | 266 | PF00069 | 0.591 |
MOD_CK1_1 | 273 | 279 | PF00069 | 0.577 |
MOD_CK1_1 | 471 | 477 | PF00069 | 0.672 |
MOD_CK1_1 | 490 | 496 | PF00069 | 0.591 |
MOD_CK1_1 | 51 | 57 | PF00069 | 0.477 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.554 |
MOD_CK2_1 | 1 | 7 | PF00069 | 0.462 |
MOD_CK2_1 | 233 | 239 | PF00069 | 0.316 |
MOD_CK2_1 | 241 | 247 | PF00069 | 0.483 |
MOD_CK2_1 | 532 | 538 | PF00069 | 0.542 |
MOD_CK2_1 | 79 | 85 | PF00069 | 0.577 |
MOD_DYRK1A_RPxSP_1 | 266 | 270 | PF00069 | 0.516 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.609 |
MOD_GlcNHglycan | 289 | 292 | PF01048 | 0.478 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.565 |
MOD_GlcNHglycan | 470 | 473 | PF01048 | 0.593 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.466 |
MOD_GlcNHglycan | 620 | 623 | PF01048 | 0.424 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.583 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.699 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.551 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.686 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.523 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.420 |
MOD_GSK3_1 | 407 | 414 | PF00069 | 0.498 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.559 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.757 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.609 |
MOD_GSK3_1 | 470 | 477 | PF00069 | 0.689 |
MOD_GSK3_1 | 487 | 494 | PF00069 | 0.509 |
MOD_GSK3_1 | 608 | 615 | PF00069 | 0.331 |
MOD_N-GLC_1 | 172 | 177 | PF02516 | 0.293 |
MOD_N-GLC_1 | 423 | 428 | PF02516 | 0.486 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.529 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.321 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.343 |
MOD_NEK2_1 | 233 | 238 | PF00069 | 0.500 |
MOD_NEK2_1 | 264 | 269 | PF00069 | 0.643 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.264 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.436 |
MOD_NEK2_1 | 417 | 422 | PF00069 | 0.542 |
MOD_NEK2_1 | 446 | 451 | PF00069 | 0.657 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.472 |
MOD_NEK2_1 | 520 | 525 | PF00069 | 0.459 |
MOD_NEK2_1 | 618 | 623 | PF00069 | 0.563 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.626 |
MOD_NEK2_2 | 123 | 128 | PF00069 | 0.501 |
MOD_PIKK_1 | 151 | 157 | PF00454 | 0.395 |
MOD_PIKK_1 | 165 | 171 | PF00454 | 0.224 |
MOD_PIKK_1 | 333 | 339 | PF00454 | 0.272 |
MOD_PIKK_1 | 634 | 640 | PF00454 | 0.486 |
MOD_PIKK_1 | 67 | 73 | PF00454 | 0.498 |
MOD_PKA_1 | 67 | 73 | PF00069 | 0.498 |
MOD_PKA_2 | 276 | 282 | PF00069 | 0.665 |
MOD_PKA_2 | 557 | 563 | PF00069 | 0.585 |
MOD_PKA_2 | 571 | 577 | PF00069 | 0.428 |
MOD_PKA_2 | 583 | 589 | PF00069 | 0.549 |
MOD_PKA_2 | 598 | 604 | PF00069 | 0.502 |
MOD_PKA_2 | 67 | 73 | PF00069 | 0.516 |
MOD_Plk_1 | 172 | 178 | PF00069 | 0.293 |
MOD_Plk_4 | 1 | 7 | PF00069 | 0.396 |
MOD_Plk_4 | 138 | 144 | PF00069 | 0.252 |
MOD_Plk_4 | 36 | 42 | PF00069 | 0.443 |
MOD_Plk_4 | 51 | 57 | PF00069 | 0.477 |
MOD_Plk_4 | 583 | 589 | PF00069 | 0.407 |
MOD_Plk_4 | 620 | 626 | PF00069 | 0.530 |
MOD_ProDKin_1 | 257 | 263 | PF00069 | 0.526 |
MOD_ProDKin_1 | 266 | 272 | PF00069 | 0.482 |
MOD_ProDKin_1 | 299 | 305 | PF00069 | 0.295 |
MOD_ProDKin_1 | 439 | 445 | PF00069 | 0.791 |
MOD_ProDKin_1 | 487 | 493 | PF00069 | 0.563 |
MOD_ProDKin_1 | 522 | 528 | PF00069 | 0.579 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.444 |
MOD_SUMO_for_1 | 602 | 605 | PF00179 | 0.367 |
TRG_DiLeu_BaEn_4 | 221 | 227 | PF01217 | 0.447 |
TRG_DiLeu_BaLyEn_6 | 224 | 229 | PF01217 | 0.387 |
TRG_DiLeu_BaLyEn_6 | 324 | 329 | PF01217 | 0.403 |
TRG_ENDOCYTIC_2 | 159 | 162 | PF00928 | 0.346 |
TRG_ENDOCYTIC_2 | 206 | 209 | PF00928 | 0.534 |
TRG_ENDOCYTIC_2 | 397 | 400 | PF00928 | 0.425 |
TRG_ENDOCYTIC_2 | 570 | 573 | PF00928 | 0.456 |
TRG_ER_diArg_1 | 26 | 28 | PF00400 | 0.369 |
TRG_ER_diArg_1 | 265 | 268 | PF00400 | 0.513 |
TRG_ER_diArg_1 | 648 | 650 | PF00400 | 0.445 |
TRG_ER_diArg_1 | 66 | 68 | PF00400 | 0.585 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4C1 | Leptomonas seymouri | 37% | 98% |
A0A3S7WTW1 | Leishmania donovani | 68% | 100% |
E9AQM2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 68% | 100% |
Q4QEV6 | Leishmania major | 69% | 99% |