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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0005694 | chromosome | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: A4HGN2
Term | Name | Level | Count |
---|---|---|---|
GO:0007049 | cell cycle | 2 | 6 |
GO:0009987 | cellular process | 1 | 7 |
GO:0022414 | reproductive process | 1 | 7 |
GO:0051321 | meiotic cell cycle | 2 | 6 |
GO:0000075 | cell cycle checkpoint signaling | 4 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006259 | DNA metabolic process | 4 | 1 |
GO:0006310 | DNA recombination | 5 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0007131 | reciprocal meiotic recombination | 3 | 1 |
GO:0007165 | signal transduction | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0010564 | regulation of cell cycle process | 5 | 1 |
GO:0010639 | negative regulation of organelle organization | 6 | 1 |
GO:0010948 | negative regulation of cell cycle process | 6 | 1 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0033043 | regulation of organelle organization | 5 | 1 |
GO:0033313 | meiotic cell cycle checkpoint signaling | 3 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0035556 | intracellular signal transduction | 3 | 1 |
GO:0035825 | homologous recombination | 6 | 1 |
GO:0040020 | regulation of meiotic nuclear division | 5 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0045786 | negative regulation of cell cycle | 5 | 1 |
GO:0045835 | negative regulation of meiotic nuclear division | 6 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0048519 | negative regulation of biological process | 3 | 1 |
GO:0048523 | negative regulation of cellular process | 4 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051128 | regulation of cellular component organization | 4 | 1 |
GO:0051129 | negative regulation of cellular component organization | 5 | 1 |
GO:0051445 | regulation of meiotic cell cycle | 4 | 1 |
GO:0051447 | negative regulation of meiotic cell cycle | 5 | 1 |
GO:0051598 | meiotic recombination checkpoint signaling | 4 | 1 |
GO:0051726 | regulation of cell cycle | 4 | 1 |
GO:0051783 | regulation of nuclear division | 6 | 1 |
GO:0051784 | negative regulation of nuclear division | 7 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:0140527 | reciprocal homologous recombination | 7 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1901987 | regulation of cell cycle phase transition | 6 | 1 |
GO:1901988 | negative regulation of cell cycle phase transition | 7 | 1 |
GO:1903046 | meiotic cell cycle process | 2 | 1 |
GO:2000241 | regulation of reproductive process | 3 | 1 |
GO:2000242 | negative regulation of reproductive process | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 8 |
GO:0003824 | catalytic activity | 1 | 8 |
GO:0005488 | binding | 1 | 8 |
GO:0005524 | ATP binding | 5 | 8 |
GO:0016462 | pyrophosphatase activity | 5 | 8 |
GO:0016787 | hydrolase activity | 2 | 8 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 8 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 8 |
GO:0016887 | ATP hydrolysis activity | 7 | 8 |
GO:0017076 | purine nucleotide binding | 4 | 8 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 8 |
GO:0030554 | adenyl nucleotide binding | 5 | 8 |
GO:0032553 | ribonucleotide binding | 3 | 8 |
GO:0032555 | purine ribonucleotide binding | 4 | 8 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 8 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 8 |
GO:0036094 | small molecule binding | 2 | 8 |
GO:0043167 | ion binding | 2 | 8 |
GO:0043168 | anion binding | 3 | 8 |
GO:0097159 | organic cyclic compound binding | 2 | 8 |
GO:0097367 | carbohydrate derivative binding | 2 | 8 |
GO:1901265 | nucleoside phosphate binding | 3 | 8 |
GO:1901363 | heterocyclic compound binding | 2 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 69 | 73 | PF00656 | 0.490 |
CLV_NRD_NRD_1 | 52 | 54 | PF00675 | 0.463 |
CLV_PCSK_KEX2_1 | 185 | 187 | PF00082 | 0.384 |
CLV_PCSK_KEX2_1 | 267 | 269 | PF00082 | 0.399 |
CLV_PCSK_KEX2_1 | 355 | 357 | PF00082 | 0.369 |
CLV_PCSK_KEX2_1 | 52 | 54 | PF00082 | 0.463 |
CLV_PCSK_PC1ET2_1 | 185 | 187 | PF00082 | 0.384 |
CLV_PCSK_PC1ET2_1 | 267 | 269 | PF00082 | 0.399 |
CLV_PCSK_PC1ET2_1 | 355 | 357 | PF00082 | 0.369 |
CLV_PCSK_SKI1_1 | 212 | 216 | PF00082 | 0.309 |
CLV_PCSK_SKI1_1 | 267 | 271 | PF00082 | 0.369 |
CLV_PCSK_SKI1_1 | 513 | 517 | PF00082 | 0.384 |
CLV_PCSK_SKI1_1 | 52 | 56 | PF00082 | 0.439 |
DEG_APCC_DBOX_1 | 245 | 253 | PF00400 | 0.369 |
DEG_APCC_DBOX_1 | 557 | 565 | PF00400 | 0.462 |
DOC_ANK_TNKS_1 | 411 | 418 | PF00023 | 0.564 |
DOC_CDC14_PxL_1 | 515 | 523 | PF14671 | 0.365 |
DOC_CDC14_PxL_1 | 70 | 78 | PF14671 | 0.468 |
DOC_CYCLIN_RxL_1 | 364 | 374 | PF00134 | 0.383 |
DOC_MAPK_gen_1 | 16 | 26 | PF00069 | 0.339 |
DOC_MAPK_MEF2A_6 | 19 | 26 | PF00069 | 0.441 |
DOC_MAPK_MEF2A_6 | 78 | 86 | PF00069 | 0.296 |
DOC_PP1_RVXF_1 | 210 | 217 | PF00149 | 0.419 |
DOC_PP4_FxxP_1 | 216 | 219 | PF00568 | 0.369 |
DOC_PP4_FxxP_1 | 457 | 460 | PF00568 | 0.611 |
DOC_SPAK_OSR1_1 | 367 | 371 | PF12202 | 0.346 |
DOC_USP7_MATH_1 | 123 | 127 | PF00917 | 0.606 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.711 |
DOC_USP7_MATH_1 | 161 | 165 | PF00917 | 0.416 |
DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.399 |
DOC_USP7_MATH_1 | 310 | 314 | PF00917 | 0.369 |
DOC_USP7_MATH_1 | 389 | 393 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 579 | 583 | PF00917 | 0.411 |
DOC_WW_Pin1_4 | 116 | 121 | PF00397 | 0.432 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.443 |
DOC_WW_Pin1_4 | 155 | 160 | PF00397 | 0.465 |
DOC_WW_Pin1_4 | 201 | 206 | PF00397 | 0.393 |
DOC_WW_Pin1_4 | 464 | 469 | PF00397 | 0.621 |
DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.662 |
LIG_14-3-3_CanoR_1 | 238 | 244 | PF00244 | 0.399 |
LIG_14-3-3_CanoR_1 | 260 | 269 | PF00244 | 0.309 |
LIG_14-3-3_CanoR_1 | 27 | 35 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 4 | 13 | PF00244 | 0.659 |
LIG_14-3-3_CanoR_1 | 52 | 61 | PF00244 | 0.345 |
LIG_BIR_III_2 | 72 | 76 | PF00653 | 0.500 |
LIG_BRCT_BRCA1_1 | 180 | 184 | PF00533 | 0.437 |
LIG_BRCT_BRCA1_1 | 258 | 262 | PF00533 | 0.309 |
LIG_BRCT_BRCA1_1 | 453 | 457 | PF00533 | 0.665 |
LIG_BRCT_BRCA1_2 | 453 | 459 | PF00533 | 0.612 |
LIG_Clathr_ClatBox_1 | 21 | 25 | PF01394 | 0.415 |
LIG_EH1_1 | 493 | 501 | PF00400 | 0.479 |
LIG_eIF4E_1 | 244 | 250 | PF01652 | 0.369 |
LIG_eIF4E_1 | 494 | 500 | PF01652 | 0.468 |
LIG_FHA_1 | 336 | 342 | PF00498 | 0.331 |
LIG_FHA_1 | 345 | 351 | PF00498 | 0.343 |
LIG_FHA_1 | 389 | 395 | PF00498 | 0.740 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.476 |
LIG_FHA_2 | 26 | 32 | PF00498 | 0.458 |
LIG_FHA_2 | 320 | 326 | PF00498 | 0.309 |
LIG_FHA_2 | 96 | 102 | PF00498 | 0.460 |
LIG_GBD_Chelix_1 | 231 | 239 | PF00786 | 0.369 |
LIG_Integrin_isoDGR_2 | 511 | 513 | PF01839 | 0.447 |
LIG_LIR_Apic_2 | 454 | 460 | PF02991 | 0.608 |
LIG_LIR_Gen_1 | 166 | 174 | PF02991 | 0.382 |
LIG_LIR_Gen_1 | 17 | 26 | PF02991 | 0.435 |
LIG_LIR_Gen_1 | 271 | 280 | PF02991 | 0.224 |
LIG_LIR_Gen_1 | 44 | 50 | PF02991 | 0.494 |
LIG_LIR_Gen_1 | 96 | 105 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 166 | 172 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 17 | 23 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 271 | 276 | PF02991 | 0.224 |
LIG_LIR_Nem_3 | 32 | 38 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 421 | 425 | PF02991 | 0.591 |
LIG_LIR_Nem_3 | 44 | 48 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 96 | 100 | PF02991 | 0.332 |
LIG_Pex14_2 | 258 | 262 | PF04695 | 0.309 |
LIG_SH2_CRK | 372 | 376 | PF00017 | 0.460 |
LIG_SH2_NCK_1 | 372 | 376 | PF00017 | 0.406 |
LIG_SH2_PTP2 | 45 | 48 | PF00017 | 0.430 |
LIG_SH2_SRC | 560 | 563 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 191 | 194 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 20 | 23 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 45 | 48 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 494 | 497 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 560 | 563 | PF00017 | 0.455 |
LIG_SH3_3 | 356 | 362 | PF00018 | 0.399 |
LIG_SH3_3 | 381 | 387 | PF00018 | 0.499 |
LIG_SH3_3 | 392 | 398 | PF00018 | 0.620 |
LIG_SH3_3 | 471 | 477 | PF00018 | 0.737 |
LIG_SH3_3 | 548 | 554 | PF00018 | 0.525 |
LIG_SH3_3 | 58 | 64 | PF00018 | 0.473 |
LIG_SH3_3 | 7 | 13 | PF00018 | 0.649 |
LIG_SH3_3 | 86 | 92 | PF00018 | 0.396 |
LIG_SH3_5 | 556 | 560 | PF00018 | 0.487 |
LIG_SUMO_SIM_par_1 | 20 | 25 | PF11976 | 0.431 |
LIG_SUMO_SIM_par_1 | 268 | 274 | PF11976 | 0.224 |
LIG_SUMO_SIM_par_1 | 332 | 339 | PF11976 | 0.368 |
LIG_SUMO_SIM_par_1 | 66 | 72 | PF11976 | 0.469 |
LIG_TRAF2_1 | 374 | 377 | PF00917 | 0.349 |
LIG_TRAF2_1 | 567 | 570 | PF00917 | 0.346 |
LIG_TRFH_1 | 155 | 159 | PF08558 | 0.328 |
LIG_TYR_ITIM | 370 | 375 | PF00017 | 0.354 |
LIG_WRC_WIRS_1 | 527 | 532 | PF05994 | 0.378 |
MOD_CDK_SPxxK_3 | 9 | 16 | PF00069 | 0.472 |
MOD_CK1_1 | 153 | 159 | PF00069 | 0.450 |
MOD_CK1_1 | 256 | 262 | PF00069 | 0.309 |
MOD_CK1_1 | 424 | 430 | PF00069 | 0.595 |
MOD_CK1_1 | 467 | 473 | PF00069 | 0.719 |
MOD_CK1_1 | 529 | 535 | PF00069 | 0.690 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.576 |
MOD_CK2_1 | 371 | 377 | PF00069 | 0.433 |
MOD_CK2_1 | 95 | 101 | PF00069 | 0.461 |
MOD_Cter_Amidation | 265 | 268 | PF01082 | 0.399 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.608 |
MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.411 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.309 |
MOD_GlcNHglycan | 302 | 305 | PF01048 | 0.323 |
MOD_GlcNHglycan | 401 | 404 | PF01048 | 0.707 |
MOD_GlcNHglycan | 474 | 477 | PF01048 | 0.752 |
MOD_GlcNHglycan | 489 | 492 | PF01048 | 0.636 |
MOD_GlcNHglycan | 533 | 536 | PF01048 | 0.617 |
MOD_GlcNHglycan | 540 | 543 | PF01048 | 0.679 |
MOD_GlcNHglycan | 547 | 550 | PF01048 | 0.751 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.618 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.618 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.579 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.431 |
MOD_GSK3_1 | 187 | 194 | PF00069 | 0.314 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.269 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.402 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.324 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.353 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.344 |
MOD_GSK3_1 | 447 | 454 | PF00069 | 0.577 |
MOD_GSK3_1 | 466 | 473 | PF00069 | 0.737 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.332 |
MOD_GSK3_1 | 526 | 533 | PF00069 | 0.462 |
MOD_N-GLC_1 | 150 | 155 | PF02516 | 0.430 |
MOD_N-GLC_1 | 339 | 344 | PF02516 | 0.309 |
MOD_N-GLC_1 | 447 | 452 | PF02516 | 0.561 |
MOD_N-GLC_1 | 545 | 550 | PF02516 | 0.490 |
MOD_NEK2_1 | 239 | 244 | PF00069 | 0.369 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.309 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.559 |
MOD_NEK2_1 | 336 | 341 | PF00069 | 0.313 |
MOD_NEK2_1 | 371 | 376 | PF00069 | 0.405 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.429 |
MOD_NEK2_1 | 530 | 535 | PF00069 | 0.594 |
MOD_NEK2_2 | 310 | 315 | PF00069 | 0.369 |
MOD_PIKK_1 | 319 | 325 | PF00454 | 0.309 |
MOD_PKA_1 | 52 | 58 | PF00069 | 0.347 |
MOD_PKA_2 | 26 | 32 | PF00069 | 0.458 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.797 |
MOD_PKA_2 | 300 | 306 | PF00069 | 0.318 |
MOD_PKA_2 | 452 | 458 | PF00069 | 0.541 |
MOD_PKA_2 | 52 | 58 | PF00069 | 0.347 |
MOD_Plk_1 | 150 | 156 | PF00069 | 0.420 |
MOD_Plk_1 | 36 | 42 | PF00069 | 0.450 |
MOD_Plk_1 | 87 | 93 | PF00069 | 0.480 |
MOD_Plk_2-3 | 187 | 193 | PF00069 | 0.420 |
MOD_Plk_4 | 187 | 193 | PF00069 | 0.495 |
MOD_Plk_4 | 239 | 245 | PF00069 | 0.411 |
MOD_Plk_4 | 253 | 259 | PF00069 | 0.228 |
MOD_Plk_4 | 37 | 43 | PF00069 | 0.331 |
MOD_Plk_4 | 389 | 395 | PF00069 | 0.618 |
MOD_Plk_4 | 495 | 501 | PF00069 | 0.402 |
MOD_ProDKin_1 | 116 | 122 | PF00069 | 0.433 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.435 |
MOD_ProDKin_1 | 155 | 161 | PF00069 | 0.460 |
MOD_ProDKin_1 | 201 | 207 | PF00069 | 0.396 |
MOD_ProDKin_1 | 464 | 470 | PF00069 | 0.620 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.654 |
MOD_SUMO_rev_2 | 9 | 18 | PF00179 | 0.464 |
TRG_DiLeu_BaEn_1 | 37 | 42 | PF01217 | 0.465 |
TRG_DiLeu_BaLyEn_6 | 72 | 77 | PF01217 | 0.489 |
TRG_ENDOCYTIC_2 | 20 | 23 | PF00928 | 0.466 |
TRG_ENDOCYTIC_2 | 372 | 375 | PF00928 | 0.456 |
TRG_ENDOCYTIC_2 | 422 | 425 | PF00928 | 0.526 |
TRG_ENDOCYTIC_2 | 45 | 48 | PF00928 | 0.430 |
TRG_ER_diArg_1 | 52 | 54 | PF00400 | 0.417 |
TRG_NES_CRM1_1 | 37 | 49 | PF08389 | 0.461 |
TRG_Pf-PMV_PEXEL_1 | 229 | 233 | PF00026 | 0.369 |
TRG_Pf-PMV_PEXEL_1 | 277 | 281 | PF00026 | 0.224 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P830 | Leptomonas seymouri | 55% | 100% |
A0A3Q8IEP0 | Leishmania donovani | 80% | 100% |
E9AHG7 | Leishmania infantum | 80% | 100% |
E9AZZ8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% |
Q4Q887 | Leishmania major | 82% | 100% |
V5BAN2 | Trypanosoma cruzi | 45% | 96% |