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:0000228 | nuclear chromosome | 6 | 2 |
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 |
Related structures:
AlphaFold database: Q4QEV6
Term | Name | Level | Count |
---|---|---|---|
GO:0000706 | meiotic DNA double-strand break processing | 3 | 2 |
GO:0000729 | DNA double-strand break processing | 5 | 2 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 6 |
GO:0006259 | DNA metabolic process | 4 | 6 |
GO:0006310 | DNA recombination | 5 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 6 |
GO:0006807 | nitrogen compound metabolic process | 2 | 6 |
GO:0007131 | reciprocal meiotic recombination | 3 | 2 |
GO:0008152 | metabolic process | 1 | 6 |
GO:0009987 | cellular process | 1 | 6 |
GO:0022402 | cell cycle process | 2 | 2 |
GO:0022414 | reproductive process | 1 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 6 |
GO:0035825 | homologous recombination | 6 | 2 |
GO:0042138 | meiotic DNA double-strand break formation | 4 | 2 |
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:0061982 | meiosis I cell cycle process | 3 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 6 |
GO:0090304 | nucleic acid metabolic process | 4 | 6 |
GO:0090305 | nucleic acid phosphodiester bond hydrolysis | 5 | 2 |
GO:0140527 | reciprocal homologous recombination | 7 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 6 |
GO:1903046 | meiotic cell cycle process | 2 | 2 |
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 | 417 | 421 | PF00656 | 0.615 |
CLV_C14_Caspase3-7 | 501 | 505 | PF00656 | 0.558 |
CLV_NRD_NRD_1 | 127 | 129 | PF00675 | 0.437 |
CLV_NRD_NRD_1 | 27 | 29 | PF00675 | 0.376 |
CLV_NRD_NRD_1 | 344 | 346 | PF00675 | 0.445 |
CLV_NRD_NRD_1 | 502 | 504 | PF00675 | 0.487 |
CLV_NRD_NRD_1 | 543 | 545 | PF00675 | 0.665 |
CLV_NRD_NRD_1 | 627 | 629 | PF00675 | 0.699 |
CLV_NRD_NRD_1 | 647 | 649 | PF00675 | 0.277 |
CLV_NRD_NRD_1 | 68 | 70 | PF00675 | 0.700 |
CLV_PCSK_KEX2_1 | 127 | 129 | PF00082 | 0.437 |
CLV_PCSK_KEX2_1 | 27 | 29 | PF00082 | 0.376 |
CLV_PCSK_KEX2_1 | 344 | 346 | PF00082 | 0.445 |
CLV_PCSK_KEX2_1 | 418 | 420 | PF00082 | 0.532 |
CLV_PCSK_KEX2_1 | 46 | 48 | PF00082 | 0.534 |
CLV_PCSK_KEX2_1 | 502 | 504 | PF00082 | 0.500 |
CLV_PCSK_KEX2_1 | 542 | 544 | PF00082 | 0.701 |
CLV_PCSK_KEX2_1 | 626 | 628 | PF00082 | 0.666 |
CLV_PCSK_KEX2_1 | 647 | 649 | PF00082 | 0.423 |
CLV_PCSK_KEX2_1 | 67 | 69 | PF00082 | 0.707 |
CLV_PCSK_PC1ET2_1 | 418 | 420 | PF00082 | 0.505 |
CLV_PCSK_PC1ET2_1 | 46 | 48 | PF00082 | 0.522 |
CLV_PCSK_PC7_1 | 414 | 420 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.677 |
CLV_PCSK_SKI1_1 | 283 | 287 | PF00082 | 0.632 |
CLV_PCSK_SKI1_1 | 344 | 348 | PF00082 | 0.448 |
CLV_PCSK_SKI1_1 | 46 | 50 | PF00082 | 0.555 |
CLV_Separin_Metazoa | 24 | 28 | PF03568 | 0.400 |
DEG_APCC_DBOX_1 | 133 | 141 | PF00400 | 0.308 |
DEG_APCC_DBOX_1 | 320 | 328 | PF00400 | 0.364 |
DEG_APCC_DBOX_1 | 343 | 351 | PF00400 | 0.444 |
DEG_SCF_TRCP1_1 | 420 | 425 | PF00400 | 0.574 |
DOC_CDC14_PxL_1 | 396 | 404 | PF14671 | 0.451 |
DOC_MAPK_gen_1 | 184 | 192 | PF00069 | 0.308 |
DOC_MAPK_gen_1 | 27 | 33 | PF00069 | 0.378 |
DOC_MAPK_MEF2A_6 | 326 | 333 | PF00069 | 0.370 |
DOC_MAPK_RevD_3 | 31 | 47 | PF00069 | 0.442 |
DOC_PP2B_LxvP_1 | 183 | 186 | PF13499 | 0.308 |
DOC_PP2B_LxvP_1 | 41 | 44 | PF13499 | 0.523 |
DOC_PP4_FxxP_1 | 298 | 301 | PF00568 | 0.360 |
DOC_USP7_MATH_1 | 123 | 127 | PF00917 | 0.659 |
DOC_USP7_MATH_1 | 258 | 262 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 379 | 383 | PF00917 | 0.568 |
DOC_USP7_MATH_1 | 386 | 390 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 461 | 465 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 467 | 471 | PF00917 | 0.733 |
DOC_USP7_MATH_1 | 490 | 494 | PF00917 | 0.671 |
DOC_USP7_MATH_1 | 521 | 525 | PF00917 | 0.633 |
DOC_USP7_UBL2_3 | 530 | 534 | PF12436 | 0.557 |
DOC_WW_Pin1_4 | 438 | 443 | PF00397 | 0.802 |
DOC_WW_Pin1_4 | 486 | 491 | PF00397 | 0.577 |
DOC_WW_Pin1_4 | 522 | 527 | PF00397 | 0.625 |
DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.461 |
LIG_14-3-3_CanoR_1 | 122 | 130 | PF00244 | 0.490 |
LIG_14-3-3_CanoR_1 | 164 | 172 | PF00244 | 0.406 |
LIG_14-3-3_CanoR_1 | 276 | 285 | PF00244 | 0.622 |
LIG_14-3-3_CanoR_1 | 288 | 298 | PF00244 | 0.432 |
LIG_14-3-3_CanoR_1 | 377 | 386 | PF00244 | 0.584 |
LIG_14-3-3_CanoR_1 | 520 | 526 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 554 | 558 | PF00244 | 0.596 |
LIG_14-3-3_CanoR_1 | 568 | 572 | PF00244 | 0.686 |
LIG_14-3-3_CanoR_1 | 580 | 584 | PF00244 | 0.467 |
LIG_14-3-3_CanoR_1 | 595 | 599 | PF00244 | 0.307 |
LIG_14-3-3_CanoR_1 | 86 | 96 | PF00244 | 0.584 |
LIG_Actin_WH2_2 | 505 | 522 | PF00022 | 0.360 |
LIG_EVH1_2 | 633 | 637 | PF00568 | 0.451 |
LIG_FHA_1 | 166 | 172 | PF00498 | 0.395 |
LIG_FHA_1 | 379 | 385 | PF00498 | 0.418 |
LIG_FHA_1 | 407 | 413 | PF00498 | 0.441 |
LIG_FHA_1 | 615 | 621 | PF00498 | 0.468 |
LIG_FHA_2 | 152 | 158 | PF00498 | 0.308 |
LIG_FHA_2 | 276 | 282 | PF00498 | 0.561 |
LIG_FHA_2 | 499 | 505 | PF00498 | 0.465 |
LIG_Integrin_RGD_1 | 149 | 151 | PF01839 | 0.340 |
LIG_LIR_Apic_2 | 394 | 400 | PF02991 | 0.447 |
LIG_LIR_Apic_2 | 603 | 609 | PF02991 | 0.500 |
LIG_LIR_Gen_1 | 157 | 166 | PF02991 | 0.308 |
LIG_LIR_Gen_1 | 2 | 13 | PF02991 | 0.468 |
LIG_LIR_LC3C_4 | 230 | 235 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 141 | 147 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 157 | 163 | PF02991 | 0.264 |
LIG_LIR_Nem_3 | 2 | 8 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 393 | 399 | PF02991 | 0.587 |
LIG_LIR_Nem_3 | 401 | 407 | PF02991 | 0.424 |
LIG_MYND_1 | 325 | 329 | PF01753 | 0.357 |
LIG_NRBOX | 36 | 42 | PF00104 | 0.483 |
LIG_NRBOX | 514 | 520 | PF00104 | 0.494 |
LIG_SH2_CRK | 160 | 164 | PF00017 | 0.308 |
LIG_SH2_CRK | 606 | 610 | PF00017 | 0.529 |
LIG_SH2_CRK | 72 | 76 | PF00017 | 0.652 |
LIG_SH2_GRB2like | 610 | 613 | PF00017 | 0.433 |
LIG_SH2_NCK_1 | 606 | 610 | PF00017 | 0.529 |
LIG_SH2_STAP1 | 610 | 614 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 199 | 202 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 32 | 35 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 606 | 609 | PF00017 | 0.457 |
LIG_SH3_3 | 429 | 435 | PF00018 | 0.640 |
LIG_SH3_3 | 91 | 97 | PF00018 | 0.662 |
LIG_SH3_CIN85_PxpxPR_1 | 71 | 76 | PF14604 | 0.573 |
LIG_SUMO_SIM_par_1 | 136 | 142 | PF11976 | 0.384 |
LIG_SUMO_SIM_par_1 | 306 | 311 | PF11976 | 0.325 |
LIG_TRAF2_1 | 219 | 222 | PF00917 | 0.521 |
LIG_TYR_ITIM | 158 | 163 | PF00017 | 0.308 |
LIG_UBA3_1 | 40 | 46 | PF00899 | 0.503 |
MOD_CK1_1 | 126 | 132 | PF00069 | 0.512 |
MOD_CK1_1 | 261 | 267 | PF00069 | 0.629 |
MOD_CK1_1 | 272 | 278 | PF00069 | 0.620 |
MOD_CK1_1 | 289 | 295 | PF00069 | 0.539 |
MOD_CK1_1 | 391 | 397 | PF00069 | 0.432 |
MOD_CK1_1 | 463 | 469 | PF00069 | 0.605 |
MOD_CK1_1 | 489 | 495 | PF00069 | 0.632 |
MOD_CK1_1 | 567 | 573 | PF00069 | 0.527 |
MOD_CK2_1 | 1 | 7 | PF00069 | 0.488 |
MOD_CK2_1 | 275 | 281 | PF00069 | 0.568 |
MOD_CK2_1 | 547 | 553 | PF00069 | 0.594 |
MOD_Cter_Amidation | 540 | 543 | PF01082 | 0.575 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.414 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.638 |
MOD_GlcNHglycan | 271 | 274 | PF01048 | 0.659 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.645 |
MOD_GlcNHglycan | 388 | 391 | PF01048 | 0.596 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.591 |
MOD_GlcNHglycan | 424 | 427 | PF01048 | 0.645 |
MOD_GlcNHglycan | 429 | 432 | PF01048 | 0.574 |
MOD_GlcNHglycan | 465 | 468 | PF01048 | 0.579 |
MOD_GlcNHglycan | 476 | 479 | PF01048 | 0.622 |
MOD_GlcNHglycan | 559 | 562 | PF01048 | 0.596 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.598 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.703 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.437 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.778 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.518 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.651 |
MOD_GSK3_1 | 418 | 425 | PF00069 | 0.594 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.733 |
MOD_GSK3_1 | 463 | 470 | PF00069 | 0.604 |
MOD_GSK3_1 | 474 | 481 | PF00069 | 0.679 |
MOD_GSK3_1 | 486 | 493 | PF00069 | 0.520 |
MOD_GSK3_1 | 553 | 560 | PF00069 | 0.573 |
MOD_N-GLC_1 | 172 | 177 | PF02516 | 0.308 |
MOD_N-GLC_1 | 261 | 266 | PF02516 | 0.582 |
MOD_N-GLC_2 | 303 | 305 | PF02516 | 0.384 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.569 |
MOD_NEK2_1 | 233 | 238 | PF00069 | 0.448 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.579 |
MOD_NEK2_1 | 263 | 268 | PF00069 | 0.536 |
MOD_NEK2_1 | 269 | 274 | PF00069 | 0.607 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.478 |
MOD_NEK2_1 | 445 | 450 | PF00069 | 0.754 |
MOD_NEK2_1 | 614 | 619 | PF00069 | 0.505 |
MOD_PIKK_1 | 151 | 157 | PF00454 | 0.411 |
MOD_PIKK_1 | 165 | 171 | PF00454 | 0.231 |
MOD_PIKK_1 | 632 | 638 | PF00454 | 0.510 |
MOD_PKA_1 | 418 | 424 | PF00069 | 0.553 |
MOD_PKA_2 | 126 | 132 | PF00069 | 0.406 |
MOD_PKA_2 | 275 | 281 | PF00069 | 0.685 |
MOD_PKA_2 | 418 | 424 | PF00069 | 0.588 |
MOD_PKA_2 | 553 | 559 | PF00069 | 0.680 |
MOD_PKA_2 | 567 | 573 | PF00069 | 0.655 |
MOD_PKA_2 | 579 | 585 | PF00069 | 0.433 |
MOD_PKA_2 | 594 | 600 | PF00069 | 0.384 |
MOD_Plk_1 | 172 | 178 | PF00069 | 0.308 |
MOD_Plk_1 | 445 | 451 | PF00069 | 0.563 |
MOD_Plk_4 | 233 | 239 | PF00069 | 0.401 |
MOD_Plk_4 | 36 | 42 | PF00069 | 0.503 |
MOD_Plk_4 | 547 | 553 | PF00069 | 0.651 |
MOD_Plk_4 | 579 | 585 | PF00069 | 0.439 |
MOD_Plk_4 | 616 | 622 | PF00069 | 0.552 |
MOD_ProDKin_1 | 438 | 444 | PF00069 | 0.802 |
MOD_ProDKin_1 | 486 | 492 | PF00069 | 0.576 |
MOD_ProDKin_1 | 522 | 528 | PF00069 | 0.628 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.461 |
MOD_SUMO_for_1 | 598 | 601 | PF00179 | 0.369 |
TRG_DiLeu_BaEn_4 | 221 | 227 | PF01217 | 0.470 |
TRG_DiLeu_BaLyEn_6 | 224 | 229 | PF01217 | 0.388 |
TRG_DiLeu_BaLyEn_6 | 323 | 328 | PF01217 | 0.554 |
TRG_DiLeu_BaLyEn_6 | 342 | 347 | PF01217 | 0.249 |
TRG_ENDOCYTIC_2 | 159 | 162 | PF00928 | 0.331 |
TRG_ENDOCYTIC_2 | 396 | 399 | PF00928 | 0.574 |
TRG_ER_diArg_1 | 206 | 209 | PF00400 | 0.370 |
TRG_ER_diArg_1 | 26 | 28 | PF00400 | 0.384 |
TRG_ER_diArg_1 | 344 | 346 | PF00400 | 0.411 |
TRG_ER_diArg_1 | 435 | 438 | PF00400 | 0.580 |
TRG_ER_diArg_1 | 542 | 544 | PF00400 | 0.572 |
TRG_ER_diArg_1 | 625 | 628 | PF00400 | 0.601 |
TRG_ER_diArg_1 | 646 | 648 | PF00400 | 0.485 |
TRG_ER_diArg_1 | 66 | 69 | PF00400 | 0.671 |
TRG_NES_CRM1_1 | 19 | 35 | PF08389 | 0.370 |
TRG_Pf-PMV_PEXEL_1 | 267 | 271 | PF00026 | 0.624 |
TRG_Pf-PMV_PEXEL_1 | 544 | 548 | PF00026 | 0.646 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4C1 | Leptomonas seymouri | 37% | 97% |
A0A3S7WTW1 | Leishmania donovani | 87% | 100% |
A4H8I5 | Leishmania braziliensis | 69% | 100% |
E9AQM2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |