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: E9AHG7
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 | 148 | 152 | PF00656 | 0.590 |
CLV_C14_Caspase3-7 | 191 | 195 | PF00656 | 0.280 |
CLV_C14_Caspase3-7 | 69 | 73 | PF00656 | 0.453 |
CLV_NRD_NRD_1 | 52 | 54 | PF00675 | 0.372 |
CLV_PCSK_KEX2_1 | 186 | 188 | PF00082 | 0.345 |
CLV_PCSK_KEX2_1 | 268 | 270 | PF00082 | 0.421 |
CLV_PCSK_KEX2_1 | 356 | 358 | PF00082 | 0.285 |
CLV_PCSK_KEX2_1 | 382 | 384 | PF00082 | 0.419 |
CLV_PCSK_KEX2_1 | 52 | 54 | PF00082 | 0.372 |
CLV_PCSK_PC1ET2_1 | 186 | 188 | PF00082 | 0.345 |
CLV_PCSK_PC1ET2_1 | 268 | 270 | PF00082 | 0.361 |
CLV_PCSK_PC1ET2_1 | 356 | 358 | PF00082 | 0.285 |
CLV_PCSK_PC1ET2_1 | 382 | 384 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 213 | 217 | PF00082 | 0.309 |
CLV_PCSK_SKI1_1 | 268 | 272 | PF00082 | 0.285 |
CLV_PCSK_SKI1_1 | 515 | 519 | PF00082 | 0.358 |
DEG_APCC_DBOX_1 | 246 | 254 | PF00400 | 0.285 |
DEG_APCC_DBOX_1 | 558 | 566 | PF00400 | 0.427 |
DEG_SPOP_SBC_1 | 468 | 472 | PF00917 | 0.647 |
DEG_SPOP_SBC_1 | 5 | 9 | PF00917 | 0.589 |
DOC_CDC14_PxL_1 | 517 | 525 | PF14671 | 0.340 |
DOC_CDC14_PxL_1 | 70 | 78 | PF14671 | 0.387 |
DOC_MAPK_MEF2A_6 | 19 | 26 | PF00069 | 0.363 |
DOC_PP1_RVXF_1 | 211 | 218 | PF00149 | 0.331 |
DOC_PP4_FxxP_1 | 217 | 220 | PF00568 | 0.285 |
DOC_PP4_FxxP_1 | 552 | 555 | PF00568 | 0.404 |
DOC_SPAK_OSR1_1 | 368 | 372 | PF12202 | 0.311 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 162 | 166 | PF00917 | 0.486 |
DOC_USP7_MATH_1 | 202 | 206 | PF00917 | 0.348 |
DOC_USP7_MATH_1 | 301 | 305 | PF00917 | 0.313 |
DOC_USP7_MATH_1 | 311 | 315 | PF00917 | 0.325 |
DOC_USP7_MATH_1 | 390 | 394 | PF00917 | 0.578 |
DOC_USP7_MATH_1 | 423 | 427 | PF00917 | 0.661 |
DOC_USP7_MATH_1 | 456 | 460 | PF00917 | 0.536 |
DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.589 |
DOC_USP7_MATH_2 | 12 | 18 | PF00917 | 0.538 |
DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.387 |
DOC_WW_Pin1_4 | 483 | 488 | PF00397 | 0.684 |
DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.696 |
LIG_14-3-3_CanoR_1 | 119 | 129 | PF00244 | 0.573 |
LIG_14-3-3_CanoR_1 | 198 | 204 | PF00244 | 0.368 |
LIG_14-3-3_CanoR_1 | 239 | 245 | PF00244 | 0.361 |
LIG_14-3-3_CanoR_1 | 261 | 270 | PF00244 | 0.285 |
LIG_14-3-3_CanoR_1 | 27 | 35 | PF00244 | 0.425 |
LIG_14-3-3_CanoR_1 | 4 | 10 | PF00244 | 0.659 |
LIG_BIR_III_2 | 72 | 76 | PF00653 | 0.464 |
LIG_BRCT_BRCA1_1 | 181 | 185 | PF00533 | 0.342 |
LIG_BRCT_BRCA1_1 | 204 | 208 | PF00533 | 0.418 |
LIG_BRCT_BRCA1_1 | 259 | 263 | PF00533 | 0.285 |
LIG_Clathr_ClatBox_1 | 21 | 25 | PF01394 | 0.342 |
LIG_EH1_1 | 495 | 503 | PF00400 | 0.396 |
LIG_eIF4E_1 | 245 | 251 | PF01652 | 0.285 |
LIG_eIF4E_1 | 496 | 502 | PF01652 | 0.383 |
LIG_FHA_1 | 153 | 159 | PF00498 | 0.393 |
LIG_FHA_1 | 16 | 22 | PF00498 | 0.465 |
LIG_FHA_1 | 337 | 343 | PF00498 | 0.285 |
LIG_FHA_1 | 390 | 396 | PF00498 | 0.657 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.435 |
LIG_FHA_2 | 26 | 32 | PF00498 | 0.416 |
LIG_FHA_2 | 321 | 327 | PF00498 | 0.304 |
LIG_FHA_2 | 495 | 501 | PF00498 | 0.416 |
LIG_FHA_2 | 96 | 102 | PF00498 | 0.358 |
LIG_GBD_Chelix_1 | 232 | 240 | PF00786 | 0.361 |
LIG_GBD_Chelix_1 | 317 | 325 | PF00786 | 0.313 |
LIG_Integrin_isoDGR_2 | 513 | 515 | PF01839 | 0.359 |
LIG_LIR_Gen_1 | 167 | 175 | PF02991 | 0.342 |
LIG_LIR_Gen_1 | 17 | 26 | PF02991 | 0.373 |
LIG_LIR_Gen_1 | 210 | 217 | PF02991 | 0.319 |
LIG_LIR_Gen_1 | 44 | 50 | PF02991 | 0.403 |
LIG_LIR_Gen_1 | 96 | 105 | PF02991 | 0.364 |
LIG_LIR_LC3C_4 | 18 | 23 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 167 | 173 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 17 | 23 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 210 | 214 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 32 | 38 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 44 | 48 | PF02991 | 0.333 |
LIG_Pex14_1 | 170 | 174 | PF04695 | 0.317 |
LIG_Pex14_2 | 259 | 263 | PF04695 | 0.285 |
LIG_SH2_CRK | 373 | 377 | PF00017 | 0.417 |
LIG_SH2_PTP2 | 359 | 362 | PF00017 | 0.264 |
LIG_SH2_PTP2 | 45 | 48 | PF00017 | 0.335 |
LIG_SH2_SRC | 192 | 195 | PF00017 | 0.274 |
LIG_SH2_SRC | 561 | 564 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 192 | 195 | PF00017 | 0.331 |
LIG_SH2_STAT5 | 20 | 23 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 359 | 362 | PF00017 | 0.264 |
LIG_SH2_STAT5 | 45 | 48 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 496 | 499 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 533 | 536 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 561 | 564 | PF00017 | 0.419 |
LIG_SH3_3 | 357 | 363 | PF00018 | 0.361 |
LIG_SH3_3 | 382 | 388 | PF00018 | 0.410 |
LIG_SH3_3 | 478 | 484 | PF00018 | 0.609 |
LIG_SH3_3 | 58 | 64 | PF00018 | 0.390 |
LIG_SH3_3 | 7 | 13 | PF00018 | 0.686 |
LIG_SH3_3 | 86 | 92 | PF00018 | 0.333 |
LIG_SH3_4 | 461 | 468 | PF00018 | 0.746 |
LIG_SH3_5 | 557 | 561 | PF00018 | 0.446 |
LIG_SUMO_SIM_anti_2 | 574 | 579 | PF11976 | 0.364 |
LIG_SUMO_SIM_par_1 | 20 | 25 | PF11976 | 0.361 |
LIG_SUMO_SIM_par_1 | 333 | 340 | PF11976 | 0.284 |
LIG_SUMO_SIM_par_1 | 66 | 72 | PF11976 | 0.452 |
LIG_TYR_ITIM | 371 | 376 | PF00017 | 0.323 |
LIG_TYR_ITSM | 16 | 23 | PF00017 | 0.442 |
MOD_CK1_1 | 123 | 129 | PF00069 | 0.581 |
MOD_CK1_1 | 142 | 148 | PF00069 | 0.487 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.442 |
MOD_CK1_1 | 257 | 263 | PF00069 | 0.285 |
MOD_CK1_1 | 472 | 478 | PF00069 | 0.667 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.660 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.452 |
MOD_CK2_1 | 494 | 500 | PF00069 | 0.440 |
MOD_CK2_1 | 95 | 101 | PF00069 | 0.358 |
MOD_Cter_Amidation | 266 | 269 | PF01082 | 0.361 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.612 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.682 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.571 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.285 |
MOD_GlcNHglycan | 303 | 306 | PF01048 | 0.325 |
MOD_GlcNHglycan | 435 | 438 | PF01048 | 0.603 |
MOD_GlcNHglycan | 491 | 494 | PF01048 | 0.516 |
MOD_GlcNHglycan | 541 | 544 | PF01048 | 0.651 |
MOD_GlcNHglycan | 581 | 584 | PF01048 | 0.527 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.645 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.525 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.471 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.500 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.247 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.354 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.285 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.285 |
MOD_GSK3_1 | 468 | 475 | PF00069 | 0.678 |
MOD_GSK3_1 | 485 | 492 | PF00069 | 0.465 |
MOD_N-GLC_1 | 340 | 345 | PF02516 | 0.285 |
MOD_NEK2_1 | 197 | 202 | PF00069 | 0.392 |
MOD_NEK2_1 | 240 | 245 | PF00069 | 0.285 |
MOD_NEK2_1 | 263 | 268 | PF00069 | 0.285 |
MOD_NEK2_1 | 337 | 342 | PF00069 | 0.294 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.327 |
MOD_NEK2_1 | 529 | 534 | PF00069 | 0.491 |
MOD_NEK2_2 | 311 | 316 | PF00069 | 0.311 |
MOD_PIKK_1 | 127 | 133 | PF00454 | 0.498 |
MOD_PIKK_1 | 320 | 326 | PF00454 | 0.285 |
MOD_PKA_2 | 197 | 203 | PF00069 | 0.394 |
MOD_PKA_2 | 26 | 32 | PF00069 | 0.416 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.664 |
MOD_PKA_2 | 301 | 307 | PF00069 | 0.285 |
MOD_Plk_1 | 15 | 21 | PF00069 | 0.477 |
MOD_Plk_1 | 36 | 42 | PF00069 | 0.349 |
MOD_Plk_1 | 447 | 453 | PF00069 | 0.623 |
MOD_Plk_1 | 87 | 93 | PF00069 | 0.348 |
MOD_Plk_2-3 | 188 | 194 | PF00069 | 0.327 |
MOD_Plk_4 | 169 | 175 | PF00069 | 0.356 |
MOD_Plk_4 | 188 | 194 | PF00069 | 0.465 |
MOD_Plk_4 | 240 | 246 | PF00069 | 0.387 |
MOD_Plk_4 | 254 | 260 | PF00069 | 0.208 |
MOD_Plk_4 | 390 | 396 | PF00069 | 0.608 |
MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.383 |
MOD_ProDKin_1 | 483 | 489 | PF00069 | 0.685 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.690 |
MOD_SUMO_rev_2 | 326 | 334 | PF00179 | 0.252 |
TRG_DiLeu_BaEn_1 | 37 | 42 | PF01217 | 0.410 |
TRG_DiLeu_BaEn_4 | 447 | 453 | PF01217 | 0.623 |
TRG_DiLeu_BaLyEn_6 | 72 | 77 | PF01217 | 0.453 |
TRG_ENDOCYTIC_2 | 20 | 23 | PF00928 | 0.441 |
TRG_ENDOCYTIC_2 | 373 | 376 | PF00928 | 0.415 |
TRG_ENDOCYTIC_2 | 45 | 48 | PF00928 | 0.335 |
TRG_ER_diArg_1 | 52 | 54 | PF00400 | 0.383 |
TRG_NES_CRM1_1 | 37 | 49 | PF08389 | 0.408 |
TRG_Pf-PMV_PEXEL_1 | 230 | 234 | PF00026 | 0.285 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P830 | Leptomonas seymouri | 55% | 100% |
A0A3Q8IEP0 | Leishmania donovani | 99% | 100% |
A4HGN2 | Leishmania braziliensis | 80% | 100% |
B9L3S8 | Thermomicrobium roseum (strain ATCC 27502 / DSM 5159 / P-2) | 27% | 84% |
E9AZZ8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q4Q887 | Leishmania major | 93% | 100% |