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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005694 | chromosome | 5 | 7 |
GO:0043226 | organelle | 2 | 7 |
GO:0043228 | non-membrane-bounded organelle | 3 | 7 |
GO:0043229 | intracellular organelle | 3 | 7 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
GO:0000228 | nuclear chromosome | 6 | 1 |
Related structures:
AlphaFold database: E9AQM2
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 7 |
GO:0006259 | DNA metabolic process | 4 | 7 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 7 |
GO:0046483 | heterocycle metabolic process | 3 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:0090304 | nucleic acid metabolic process | 4 | 7 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 7 |
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 | 7 |
GO:0003676 | nucleic acid binding | 3 | 7 |
GO:0003677 | DNA binding | 4 | 7 |
GO:0003824 | catalytic activity | 1 | 7 |
GO:0003916 | DNA topoisomerase activity | 3 | 7 |
GO:0003918 | DNA topoisomerase type II (double strand cut, ATP-hydrolyzing) activity | 3 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0005524 | ATP binding | 5 | 7 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 7 |
GO:0016853 | isomerase activity | 2 | 7 |
GO:0017076 | purine nucleotide binding | 4 | 7 |
GO:0030554 | adenyl nucleotide binding | 5 | 7 |
GO:0032553 | ribonucleotide binding | 3 | 7 |
GO:0032555 | purine ribonucleotide binding | 4 | 7 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 7 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 7 |
GO:0036094 | small molecule binding | 2 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043168 | anion binding | 3 | 7 |
GO:0043169 | cation binding | 3 | 7 |
GO:0046872 | metal ion binding | 4 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:0097367 | carbohydrate derivative binding | 2 | 7 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 7 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 7 |
GO:0140657 | ATP-dependent activity | 1 | 7 |
GO:1901265 | nucleoside phosphate binding | 3 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 417 | 421 | PF00656 | 0.583 |
CLV_C14_Caspase3-7 | 501 | 505 | PF00656 | 0.413 |
CLV_C14_Caspase3-7 | 537 | 541 | PF00656 | 0.517 |
CLV_NRD_NRD_1 | 27 | 29 | PF00675 | 0.354 |
CLV_NRD_NRD_1 | 344 | 346 | PF00675 | 0.416 |
CLV_NRD_NRD_1 | 418 | 420 | PF00675 | 0.480 |
CLV_NRD_NRD_1 | 46 | 48 | PF00675 | 0.533 |
CLV_NRD_NRD_1 | 543 | 545 | PF00675 | 0.678 |
CLV_NRD_NRD_1 | 628 | 630 | PF00675 | 0.618 |
CLV_NRD_NRD_1 | 648 | 650 | PF00675 | 0.257 |
CLV_NRD_NRD_1 | 68 | 70 | PF00675 | 0.632 |
CLV_PCSK_KEX2_1 | 27 | 29 | PF00082 | 0.354 |
CLV_PCSK_KEX2_1 | 344 | 346 | PF00082 | 0.416 |
CLV_PCSK_KEX2_1 | 418 | 420 | PF00082 | 0.562 |
CLV_PCSK_KEX2_1 | 46 | 48 | PF00082 | 0.533 |
CLV_PCSK_KEX2_1 | 513 | 515 | PF00082 | 0.366 |
CLV_PCSK_KEX2_1 | 542 | 544 | PF00082 | 0.641 |
CLV_PCSK_KEX2_1 | 627 | 629 | PF00082 | 0.624 |
CLV_PCSK_KEX2_1 | 648 | 650 | PF00082 | 0.377 |
CLV_PCSK_KEX2_1 | 67 | 69 | PF00082 | 0.638 |
CLV_PCSK_PC1ET2_1 | 513 | 515 | PF00082 | 0.300 |
CLV_PCSK_PC1ET2_1 | 67 | 69 | PF00082 | 0.493 |
CLV_PCSK_PC7_1 | 414 | 420 | PF00082 | 0.454 |
CLV_PCSK_PC7_1 | 509 | 515 | PF00082 | 0.293 |
CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.505 |
CLV_PCSK_SKI1_1 | 283 | 287 | PF00082 | 0.531 |
CLV_PCSK_SKI1_1 | 344 | 348 | PF00082 | 0.408 |
CLV_Separin_Metazoa | 24 | 28 | PF03568 | 0.367 |
DEG_APCC_DBOX_1 | 133 | 141 | PF00400 | 0.280 |
DEG_APCC_DBOX_1 | 320 | 328 | PF00400 | 0.422 |
DEG_APCC_DBOX_1 | 343 | 351 | PF00400 | 0.416 |
DEG_SPOP_SBC_1 | 258 | 262 | PF00917 | 0.482 |
DOC_ANK_TNKS_1 | 242 | 249 | PF00023 | 0.447 |
DOC_CDC14_PxL_1 | 396 | 404 | PF14671 | 0.398 |
DOC_MAPK_DCC_7 | 86 | 96 | PF00069 | 0.492 |
DOC_MAPK_gen_1 | 184 | 192 | PF00069 | 0.338 |
DOC_MAPK_gen_1 | 27 | 33 | PF00069 | 0.357 |
DOC_MAPK_MEF2A_6 | 134 | 142 | PF00069 | 0.316 |
DOC_MAPK_MEF2A_6 | 326 | 333 | PF00069 | 0.384 |
DOC_MAPK_RevD_3 | 31 | 47 | PF00069 | 0.413 |
DOC_PP2B_LxvP_1 | 183 | 186 | PF13499 | 0.338 |
DOC_PP2B_LxvP_1 | 41 | 44 | PF13499 | 0.481 |
DOC_PP4_FxxP_1 | 298 | 301 | PF00568 | 0.496 |
DOC_USP7_MATH_1 | 104 | 108 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 115 | 119 | PF00917 | 0.457 |
DOC_USP7_MATH_1 | 123 | 127 | PF00917 | 0.542 |
DOC_USP7_MATH_1 | 258 | 262 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 379 | 383 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 386 | 390 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 467 | 471 | PF00917 | 0.711 |
DOC_USP7_MATH_1 | 490 | 494 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 521 | 525 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 565 | 569 | PF00917 | 0.450 |
DOC_WW_Pin1_4 | 438 | 443 | PF00397 | 0.813 |
DOC_WW_Pin1_4 | 46 | 51 | PF00397 | 0.446 |
DOC_WW_Pin1_4 | 475 | 480 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 486 | 491 | PF00397 | 0.611 |
DOC_WW_Pin1_4 | 522 | 527 | PF00397 | 0.662 |
DOC_WW_Pin1_4 | 59 | 64 | PF00397 | 0.487 |
DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.464 |
DOC_WW_Pin1_4 | 87 | 92 | PF00397 | 0.526 |
LIG_14-3-3_CanoR_1 | 122 | 128 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 164 | 172 | PF00244 | 0.423 |
LIG_14-3-3_CanoR_1 | 276 | 285 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 377 | 387 | PF00244 | 0.472 |
LIG_14-3-3_CanoR_1 | 51 | 56 | PF00244 | 0.485 |
LIG_14-3-3_CanoR_1 | 571 | 575 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 583 | 587 | PF00244 | 0.417 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.397 |
LIG_BIR_III_2 | 383 | 387 | PF00653 | 0.462 |
LIG_EVH1_2 | 634 | 638 | PF00568 | 0.430 |
LIG_FHA_1 | 166 | 172 | PF00498 | 0.335 |
LIG_FHA_1 | 618 | 624 | PF00498 | 0.479 |
LIG_FHA_2 | 152 | 158 | PF00498 | 0.280 |
LIG_FHA_2 | 18 | 24 | PF00498 | 0.327 |
LIG_FHA_2 | 499 | 505 | PF00498 | 0.449 |
LIG_Integrin_RGD_1 | 149 | 151 | PF01839 | 0.299 |
LIG_LIR_Apic_2 | 394 | 400 | PF02991 | 0.373 |
LIG_LIR_Apic_2 | 606 | 612 | PF02991 | 0.430 |
LIG_LIR_Gen_1 | 157 | 166 | PF02991 | 0.394 |
LIG_LIR_Gen_1 | 3 | 13 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 141 | 147 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 157 | 163 | PF02991 | 0.289 |
LIG_LIR_Nem_3 | 205 | 209 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 280 | 285 | PF02991 | 0.591 |
LIG_LIR_Nem_3 | 3 | 8 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 393 | 399 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 401 | 407 | PF02991 | 0.378 |
LIG_NRBOX | 36 | 42 | PF00104 | 0.551 |
LIG_NRBOX | 514 | 520 | PF00104 | 0.452 |
LIG_SH2_CRK | 160 | 164 | PF00017 | 0.322 |
LIG_SH2_CRK | 206 | 210 | PF00017 | 0.375 |
LIG_SH2_CRK | 397 | 401 | PF00017 | 0.302 |
LIG_SH2_CRK | 609 | 613 | PF00017 | 0.451 |
LIG_SH2_CRK | 72 | 76 | PF00017 | 0.584 |
LIG_SH2_NCK_1 | 397 | 401 | PF00017 | 0.302 |
LIG_SH2_NCK_1 | 609 | 613 | PF00017 | 0.451 |
LIG_SH2_NCK_1 | 72 | 76 | PF00017 | 0.487 |
LIG_SH2_STAP1 | 613 | 617 | PF00017 | 0.456 |
LIG_SH2_STAT3 | 613 | 616 | PF00017 | 0.297 |
LIG_SH2_STAT3 | 76 | 79 | PF00017 | 0.483 |
LIG_SH2_STAT5 | 199 | 202 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 32 | 35 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 499 | 502 | PF00017 | 0.307 |
LIG_SH2_STAT5 | 609 | 612 | PF00017 | 0.498 |
LIG_SH3_3 | 429 | 435 | PF00018 | 0.676 |
LIG_SH3_3 | 91 | 97 | PF00018 | 0.597 |
LIG_SUMO_SIM_anti_2 | 604 | 610 | PF11976 | 0.277 |
LIG_SUMO_SIM_par_1 | 136 | 141 | PF11976 | 0.335 |
LIG_SUMO_SIM_par_1 | 306 | 311 | PF11976 | 0.296 |
LIG_TRAF2_1 | 219 | 222 | PF00917 | 0.529 |
LIG_TYR_ITIM | 158 | 163 | PF00017 | 0.379 |
LIG_TYR_ITIM | 204 | 209 | PF00017 | 0.352 |
MOD_CDK_SPK_2 | 46 | 51 | PF00069 | 0.446 |
MOD_CK1_1 | 259 | 265 | PF00069 | 0.764 |
MOD_CK1_1 | 272 | 278 | PF00069 | 0.560 |
MOD_CK1_1 | 391 | 397 | PF00069 | 0.422 |
MOD_CK1_1 | 463 | 469 | PF00069 | 0.625 |
MOD_CK1_1 | 470 | 476 | PF00069 | 0.720 |
MOD_CK1_1 | 489 | 495 | PF00069 | 0.584 |
MOD_CK1_1 | 570 | 576 | PF00069 | 0.599 |
MOD_CK2_1 | 1 | 7 | PF00069 | 0.463 |
MOD_CK2_1 | 547 | 553 | PF00069 | 0.562 |
MOD_Cter_Amidation | 540 | 543 | PF01082 | 0.549 |
MOD_GlcNHglycan | 213 | 216 | PF01048 | 0.565 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.404 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.583 |
MOD_GlcNHglycan | 271 | 274 | PF01048 | 0.630 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.476 |
MOD_GlcNHglycan | 388 | 391 | PF01048 | 0.566 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.606 |
MOD_GlcNHglycan | 447 | 450 | PF01048 | 0.601 |
MOD_GlcNHglycan | 458 | 461 | PF01048 | 0.673 |
MOD_GlcNHglycan | 465 | 468 | PF01048 | 0.658 |
MOD_GlcNHglycan | 469 | 472 | PF01048 | 0.610 |
MOD_GlcNHglycan | 483 | 486 | PF01048 | 0.531 |
MOD_GlcNHglycan | 561 | 565 | PF01048 | 0.549 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.771 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.511 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.602 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.782 |
MOD_GSK3_1 | 463 | 470 | PF00069 | 0.653 |
MOD_GSK3_1 | 474 | 481 | PF00069 | 0.638 |
MOD_GSK3_1 | 486 | 493 | PF00069 | 0.497 |
MOD_GSK3_1 | 556 | 563 | PF00069 | 0.605 |
MOD_N-GLC_1 | 172 | 177 | PF02516 | 0.338 |
MOD_N-GLC_1 | 463 | 468 | PF02516 | 0.484 |
MOD_N-GLC_2 | 303 | 305 | PF02516 | 0.355 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.570 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.368 |
MOD_NEK2_1 | 211 | 216 | PF00069 | 0.518 |
MOD_NEK2_1 | 233 | 238 | PF00069 | 0.485 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.682 |
MOD_NEK2_1 | 269 | 274 | PF00069 | 0.555 |
MOD_NEK2_1 | 277 | 282 | PF00069 | 0.430 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.437 |
MOD_NEK2_1 | 445 | 450 | PF00069 | 0.665 |
MOD_NEK2_1 | 546 | 551 | PF00069 | 0.483 |
MOD_NEK2_1 | 617 | 622 | PF00069 | 0.529 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.532 |
MOD_NEK2_2 | 123 | 128 | PF00069 | 0.479 |
MOD_NEK2_2 | 129 | 134 | PF00069 | 0.352 |
MOD_PIKK_1 | 113 | 119 | PF00454 | 0.505 |
MOD_PIKK_1 | 151 | 157 | PF00454 | 0.315 |
MOD_PIKK_1 | 165 | 171 | PF00454 | 0.230 |
MOD_PIKK_1 | 277 | 283 | PF00454 | 0.448 |
MOD_PIKK_1 | 314 | 320 | PF00454 | 0.225 |
MOD_PIKK_1 | 633 | 639 | PF00454 | 0.479 |
MOD_PKA_1 | 418 | 424 | PF00069 | 0.525 |
MOD_PKA_2 | 275 | 281 | PF00069 | 0.636 |
MOD_PKA_2 | 418 | 424 | PF00069 | 0.676 |
MOD_PKA_2 | 570 | 576 | PF00069 | 0.419 |
MOD_PKA_2 | 582 | 588 | PF00069 | 0.536 |
MOD_Plk_1 | 172 | 178 | PF00069 | 0.338 |
MOD_Plk_1 | 547 | 553 | PF00069 | 0.477 |
MOD_Plk_2-3 | 556 | 562 | PF00069 | 0.471 |
MOD_Plk_4 | 138 | 144 | PF00069 | 0.238 |
MOD_Plk_4 | 233 | 239 | PF00069 | 0.371 |
MOD_Plk_4 | 36 | 42 | PF00069 | 0.496 |
MOD_ProDKin_1 | 438 | 444 | PF00069 | 0.813 |
MOD_ProDKin_1 | 46 | 52 | PF00069 | 0.446 |
MOD_ProDKin_1 | 475 | 481 | PF00069 | 0.659 |
MOD_ProDKin_1 | 486 | 492 | PF00069 | 0.607 |
MOD_ProDKin_1 | 522 | 528 | PF00069 | 0.665 |
MOD_ProDKin_1 | 59 | 65 | PF00069 | 0.486 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.465 |
MOD_ProDKin_1 | 87 | 93 | PF00069 | 0.526 |
MOD_SUMO_for_1 | 601 | 604 | PF00179 | 0.341 |
TRG_DiLeu_BaEn_4 | 221 | 227 | PF01217 | 0.419 |
TRG_DiLeu_BaLyEn_6 | 224 | 229 | PF01217 | 0.411 |
TRG_DiLeu_BaLyEn_6 | 323 | 328 | PF01217 | 0.387 |
TRG_DiLeu_BaLyEn_6 | 342 | 347 | PF01217 | 0.375 |
TRG_ENDOCYTIC_2 | 159 | 162 | PF00928 | 0.373 |
TRG_ENDOCYTIC_2 | 206 | 209 | PF00928 | 0.511 |
TRG_ENDOCYTIC_2 | 282 | 285 | PF00928 | 0.477 |
TRG_ENDOCYTIC_2 | 396 | 399 | PF00928 | 0.404 |
TRG_ER_diArg_1 | 26 | 28 | PF00400 | 0.363 |
TRG_ER_diArg_1 | 344 | 346 | PF00400 | 0.440 |
TRG_ER_diArg_1 | 435 | 438 | PF00400 | 0.582 |
TRG_ER_diArg_1 | 45 | 47 | PF00400 | 0.433 |
TRG_ER_diArg_1 | 542 | 544 | PF00400 | 0.549 |
TRG_ER_diArg_1 | 626 | 629 | PF00400 | 0.568 |
TRG_ER_diArg_1 | 647 | 649 | PF00400 | 0.430 |
TRG_NES_CRM1_1 | 19 | 35 | PF08389 | 0.423 |
TRG_NLS_MonoExtC_3 | 66 | 71 | PF00514 | 0.480 |
TRG_Pf-PMV_PEXEL_1 | 267 | 271 | PF00026 | 0.587 |
TRG_Pf-PMV_PEXEL_1 | 544 | 548 | PF00026 | 0.546 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4C1 | Leptomonas seymouri | 39% | 98% |
A0A3S7WTW1 | Leishmania donovani | 82% | 100% |
A4H8I5 | Leishmania braziliensis | 68% | 100% |
Q4QEV6 | Leishmania major | 84% | 100% |
V5BH86 | Trypanosoma cruzi | 29% | 100% |