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: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 | 1 |
Related structures:
AlphaFold database: E9AZZ8
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 | 7 |
GO:0003824 | catalytic activity | 1 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0005524 | ATP binding | 5 | 7 |
GO:0016462 | pyrophosphatase activity | 5 | 7 |
GO:0016787 | hydrolase activity | 2 | 7 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 7 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 7 |
GO:0016887 | ATP hydrolysis activity | 7 | 7 |
GO:0017076 | purine nucleotide binding | 4 | 7 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 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:0097159 | organic cyclic compound binding | 2 | 7 |
GO:0097367 | carbohydrate derivative binding | 2 | 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 | 147 | 151 | PF00656 | 0.596 |
CLV_C14_Caspase3-7 | 68 | 72 | PF00656 | 0.481 |
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.504 |
CLV_NRD_NRD_1 | 51 | 53 | PF00675 | 0.386 |
CLV_PCSK_KEX2_1 | 185 | 187 | PF00082 | 0.363 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.504 |
CLV_PCSK_KEX2_1 | 267 | 269 | PF00082 | 0.386 |
CLV_PCSK_KEX2_1 | 355 | 357 | PF00082 | 0.295 |
CLV_PCSK_KEX2_1 | 51 | 53 | PF00082 | 0.386 |
CLV_PCSK_PC1ET2_1 | 185 | 187 | PF00082 | 0.363 |
CLV_PCSK_PC1ET2_1 | 267 | 269 | PF00082 | 0.386 |
CLV_PCSK_PC1ET2_1 | 355 | 357 | PF00082 | 0.295 |
CLV_PCSK_SKI1_1 | 212 | 216 | PF00082 | 0.295 |
CLV_PCSK_SKI1_1 | 267 | 271 | PF00082 | 0.295 |
CLV_PCSK_SKI1_1 | 514 | 518 | PF00082 | 0.372 |
DEG_APCC_DBOX_1 | 245 | 253 | PF00400 | 0.295 |
DEG_APCC_DBOX_1 | 557 | 565 | PF00400 | 0.451 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.501 |
DEG_SPOP_SBC_1 | 468 | 472 | PF00917 | 0.639 |
DOC_ANK_TNKS_1 | 406 | 413 | PF00023 | 0.490 |
DOC_CDC14_PxL_1 | 516 | 524 | PF14671 | 0.351 |
DOC_CDC14_PxL_1 | 69 | 77 | PF14671 | 0.401 |
DOC_CYCLIN_RxL_1 | 364 | 374 | PF00134 | 0.375 |
DOC_MAPK_MEF2A_6 | 18 | 25 | PF00069 | 0.386 |
DOC_PP1_RVXF_1 | 210 | 217 | PF00149 | 0.341 |
DOC_PP4_FxxP_1 | 216 | 219 | PF00568 | 0.295 |
DOC_PP4_MxPP_1 | 465 | 468 | PF00568 | 0.485 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.647 |
DOC_USP7_MATH_1 | 201 | 205 | PF00917 | 0.361 |
DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.386 |
DOC_USP7_MATH_1 | 310 | 314 | PF00917 | 0.295 |
DOC_USP7_MATH_1 | 468 | 472 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 92 | 96 | PF00917 | 0.293 |
DOC_USP7_MATH_2 | 11 | 17 | PF00917 | 0.564 |
DOC_WW_Pin1_4 | 155 | 160 | PF00397 | 0.382 |
DOC_WW_Pin1_4 | 388 | 393 | PF00397 | 0.452 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.670 |
LIG_14-3-3_CanoR_1 | 118 | 127 | PF00244 | 0.566 |
LIG_14-3-3_CanoR_1 | 197 | 203 | PF00244 | 0.357 |
LIG_14-3-3_CanoR_1 | 2 | 11 | PF00244 | 0.666 |
LIG_14-3-3_CanoR_1 | 238 | 244 | PF00244 | 0.386 |
LIG_14-3-3_CanoR_1 | 26 | 34 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 260 | 269 | PF00244 | 0.295 |
LIG_BIR_III_2 | 71 | 75 | PF00653 | 0.492 |
LIG_BRCT_BRCA1_1 | 180 | 184 | PF00533 | 0.355 |
LIG_BRCT_BRCA1_1 | 203 | 207 | PF00533 | 0.436 |
LIG_BRCT_BRCA1_1 | 258 | 262 | PF00533 | 0.295 |
LIG_CtBP_PxDLS_1 | 66 | 70 | PF00389 | 0.292 |
LIG_EH1_1 | 494 | 502 | PF00400 | 0.406 |
LIG_eIF4E_1 | 244 | 250 | PF01652 | 0.295 |
LIG_eIF4E_1 | 495 | 501 | PF01652 | 0.395 |
LIG_FHA_1 | 152 | 158 | PF00498 | 0.406 |
LIG_FHA_1 | 336 | 342 | PF00498 | 0.317 |
LIG_FHA_1 | 389 | 395 | PF00498 | 0.718 |
LIG_FHA_2 | 25 | 31 | PF00498 | 0.449 |
LIG_FHA_2 | 320 | 326 | PF00498 | 0.295 |
LIG_GBD_Chelix_1 | 231 | 239 | PF00786 | 0.386 |
LIG_GBD_Chelix_1 | 316 | 324 | PF00786 | 0.332 |
LIG_Integrin_isoDGR_2 | 512 | 514 | PF01839 | 0.373 |
LIG_LIR_Gen_1 | 166 | 174 | PF02991 | 0.358 |
LIG_LIR_Gen_1 | 209 | 216 | PF02991 | 0.327 |
LIG_LIR_Gen_1 | 43 | 49 | PF02991 | 0.425 |
LIG_LIR_Gen_1 | 95 | 104 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 16 | 22 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 166 | 172 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 209 | 213 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 31 | 37 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 43 | 47 | PF02991 | 0.355 |
LIG_LYPXL_yS_3 | 19 | 22 | PF13949 | 0.293 |
LIG_MYND_1 | 8 | 12 | PF01753 | 0.468 |
LIG_Pex14_1 | 169 | 173 | PF04695 | 0.333 |
LIG_Pex14_2 | 258 | 262 | PF04695 | 0.295 |
LIG_SH2_CRK | 372 | 376 | PF00017 | 0.451 |
LIG_SH2_NCK_1 | 372 | 376 | PF00017 | 0.398 |
LIG_SH2_PTP2 | 358 | 361 | PF00017 | 0.274 |
LIG_SH2_PTP2 | 44 | 47 | PF00017 | 0.358 |
LIG_SH2_SRC | 560 | 563 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 103 | 106 | PF00017 | 0.235 |
LIG_SH2_STAT5 | 191 | 194 | PF00017 | 0.350 |
LIG_SH2_STAT5 | 358 | 361 | PF00017 | 0.274 |
LIG_SH2_STAT5 | 44 | 47 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 560 | 563 | PF00017 | 0.442 |
LIG_SH3_3 | 356 | 362 | PF00018 | 0.386 |
LIG_SH3_3 | 381 | 387 | PF00018 | 0.429 |
LIG_SH3_3 | 389 | 395 | PF00018 | 0.533 |
LIG_SH3_3 | 451 | 457 | PF00018 | 0.621 |
LIG_SH3_3 | 472 | 478 | PF00018 | 0.662 |
LIG_SH3_3 | 480 | 486 | PF00018 | 0.573 |
LIG_SH3_3 | 5 | 11 | PF00018 | 0.659 |
LIG_SH3_3 | 548 | 554 | PF00018 | 0.519 |
LIG_SH3_3 | 57 | 63 | PF00018 | 0.394 |
LIG_SH3_3 | 85 | 91 | PF00018 | 0.349 |
LIG_SH3_5 | 556 | 560 | PF00018 | 0.473 |
LIG_SUMO_SIM_anti_2 | 346 | 351 | PF11976 | 0.201 |
LIG_SUMO_SIM_par_1 | 19 | 24 | PF11976 | 0.383 |
LIG_SUMO_SIM_par_1 | 332 | 339 | PF11976 | 0.294 |
LIG_SUMO_SIM_par_1 | 65 | 71 | PF11976 | 0.482 |
LIG_TRAF2_1 | 374 | 377 | PF00917 | 0.342 |
LIG_TYR_ITSM | 15 | 22 | PF00017 | 0.474 |
LIG_UBA3_1 | 500 | 506 | PF00899 | 0.251 |
LIG_WW_2 | 8 | 11 | PF00397 | 0.473 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.595 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.443 |
MOD_CK1_1 | 151 | 157 | PF00069 | 0.451 |
MOD_CK1_1 | 256 | 262 | PF00069 | 0.295 |
MOD_CK1_1 | 399 | 405 | PF00069 | 0.484 |
MOD_CK1_1 | 471 | 477 | PF00069 | 0.740 |
MOD_CK2_1 | 371 | 377 | PF00069 | 0.463 |
MOD_Cter_Amidation | 265 | 268 | PF01082 | 0.386 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.650 |
MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.597 |
MOD_GlcNHglycan | 150 | 153 | PF01048 | 0.508 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.295 |
MOD_GlcNHglycan | 302 | 305 | PF01048 | 0.309 |
MOD_GlcNHglycan | 396 | 401 | PF01048 | 0.492 |
MOD_GlcNHglycan | 434 | 437 | PF01048 | 0.758 |
MOD_GlcNHglycan | 471 | 474 | PF01048 | 0.586 |
MOD_GlcNHglycan | 532 | 535 | PF01048 | 0.502 |
MOD_GlcNHglycan | 540 | 543 | PF01048 | 0.625 |
MOD_GlcNHglycan | 546 | 550 | PF01048 | 0.689 |
MOD_GlcNHglycan | 580 | 583 | PF01048 | 0.545 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.651 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.533 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.465 |
MOD_GSK3_1 | 187 | 194 | PF00069 | 0.277 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.462 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.256 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.369 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.310 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.295 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.360 |
MOD_GSK3_1 | 467 | 474 | PF00069 | 0.725 |
MOD_GSK3_1 | 484 | 491 | PF00069 | 0.540 |
MOD_N-GLC_1 | 339 | 344 | PF02516 | 0.295 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.416 |
MOD_NEK2_1 | 239 | 244 | PF00069 | 0.295 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.295 |
MOD_NEK2_1 | 336 | 341 | PF00069 | 0.304 |
MOD_NEK2_1 | 371 | 376 | PF00069 | 0.393 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.352 |
MOD_NEK2_1 | 469 | 474 | PF00069 | 0.504 |
MOD_NEK2_1 | 490 | 495 | PF00069 | 0.537 |
MOD_NEK2_2 | 310 | 315 | PF00069 | 0.295 |
MOD_PIKK_1 | 126 | 132 | PF00454 | 0.520 |
MOD_PIKK_1 | 319 | 325 | PF00454 | 0.295 |
MOD_PKA_1 | 2 | 8 | PF00069 | 0.495 |
MOD_PKA_2 | 196 | 202 | PF00069 | 0.418 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.683 |
MOD_PKA_2 | 25 | 31 | PF00069 | 0.449 |
MOD_PKA_2 | 300 | 306 | PF00069 | 0.304 |
MOD_Plk_1 | 14 | 20 | PF00069 | 0.510 |
MOD_Plk_1 | 35 | 41 | PF00069 | 0.375 |
MOD_Plk_1 | 446 | 452 | PF00069 | 0.628 |
MOD_Plk_1 | 86 | 92 | PF00069 | 0.367 |
MOD_Plk_2-3 | 187 | 193 | PF00069 | 0.345 |
MOD_Plk_4 | 168 | 174 | PF00069 | 0.332 |
MOD_Plk_4 | 187 | 193 | PF00069 | 0.480 |
MOD_Plk_4 | 239 | 245 | PF00069 | 0.397 |
MOD_Plk_4 | 253 | 259 | PF00069 | 0.214 |
MOD_Plk_4 | 36 | 42 | PF00069 | 0.315 |
MOD_ProDKin_1 | 155 | 161 | PF00069 | 0.376 |
MOD_ProDKin_1 | 388 | 394 | PF00069 | 0.453 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.669 |
MOD_SUMO_rev_2 | 325 | 333 | PF00179 | 0.265 |
TRG_DiLeu_BaEn_1 | 36 | 41 | PF01217 | 0.450 |
TRG_DiLeu_BaEn_4 | 446 | 452 | PF01217 | 0.628 |
TRG_DiLeu_BaLyEn_6 | 209 | 214 | PF01217 | 0.245 |
TRG_DiLeu_BaLyEn_6 | 71 | 76 | PF01217 | 0.481 |
TRG_ENDOCYTIC_2 | 103 | 106 | PF00928 | 0.243 |
TRG_ENDOCYTIC_2 | 19 | 22 | PF00928 | 0.482 |
TRG_ENDOCYTIC_2 | 372 | 375 | PF00928 | 0.449 |
TRG_ENDOCYTIC_2 | 44 | 47 | PF00928 | 0.358 |
TRG_ER_diArg_1 | 1 | 3 | PF00400 | 0.499 |
TRG_ER_diArg_1 | 51 | 53 | PF00400 | 0.386 |
TRG_NES_CRM1_1 | 36 | 48 | PF08389 | 0.446 |
TRG_Pf-PMV_PEXEL_1 | 229 | 233 | PF00026 | 0.295 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P830 | Leptomonas seymouri | 54% | 100% |
A0A3Q8IEP0 | Leishmania donovani | 91% | 100% |
A4HGN2 | Leishmania braziliensis | 79% | 100% |
E9AHG7 | Leishmania infantum | 91% | 100% |
Q4Q887 | Leishmania major | 90% | 100% |
Q9FGM0 | Arabidopsis thaliana | 26% | 72% |