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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: A4HB89
Term | Name | Level | Count |
---|---|---|---|
GO:0006793 | phosphorus metabolic process | 3 | 12 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016310 | phosphorylation | 5 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0005975 | carbohydrate metabolic process | 3 | 1 |
GO:0006020 | inositol metabolic process | 4 | 1 |
GO:0006066 | alcohol metabolic process | 3 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0019637 | organophosphate metabolic process | 3 | 1 |
GO:0019751 | polyol metabolic process | 4 | 1 |
GO:0032958 | inositol phosphate biosynthetic process | 5 | 1 |
GO:0043647 | inositol phosphate metabolic process | 4 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044262 | obsolete cellular carbohydrate metabolic process | 3 | 1 |
GO:0044281 | small molecule metabolic process | 2 | 1 |
GO:0044283 | small molecule biosynthetic process | 3 | 1 |
GO:0046165 | alcohol biosynthetic process | 4 | 1 |
GO:0046173 | polyol biosynthetic process | 5 | 1 |
GO:0046835 | carbohydrate phosphorylation | 4 | 1 |
GO:0052746 | obsolete inositol phosphorylation | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090407 | organophosphate biosynthetic process | 4 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
GO:1901615 | organic hydroxy compound metabolic process | 3 | 1 |
GO:1901617 | organic hydroxy compound biosynthetic process | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0016301 | kinase activity | 4 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 12 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035299 | inositol pentakisphosphate 2-kinase activity | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 218 | 222 | PF00656 | 0.497 |
CLV_C14_Caspase3-7 | 264 | 268 | PF00656 | 0.546 |
CLV_NRD_NRD_1 | 242 | 244 | PF00675 | 0.391 |
CLV_NRD_NRD_1 | 386 | 388 | PF00675 | 0.266 |
CLV_NRD_NRD_1 | 69 | 71 | PF00675 | 0.552 |
CLV_PCSK_KEX2_1 | 175 | 177 | PF00082 | 0.217 |
CLV_PCSK_KEX2_1 | 386 | 388 | PF00082 | 0.200 |
CLV_PCSK_KEX2_1 | 456 | 458 | PF00082 | 0.617 |
CLV_PCSK_PC1ET2_1 | 175 | 177 | PF00082 | 0.230 |
CLV_PCSK_PC1ET2_1 | 456 | 458 | PF00082 | 0.708 |
CLV_PCSK_SKI1_1 | 43 | 47 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 443 | 447 | PF00082 | 0.349 |
DEG_APCC_DBOX_1 | 219 | 227 | PF00400 | 0.562 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.554 |
DEG_SPOP_SBC_1 | 28 | 32 | PF00917 | 0.410 |
DOC_MAPK_gen_1 | 317 | 325 | PF00069 | 0.400 |
DOC_MAPK_MEF2A_6 | 13 | 22 | PF00069 | 0.460 |
DOC_MAPK_MEF2A_6 | 318 | 327 | PF00069 | 0.400 |
DOC_MAPK_MEF2A_6 | 375 | 383 | PF00069 | 0.501 |
DOC_MAPK_MEF2A_6 | 421 | 429 | PF00069 | 0.400 |
DOC_PP1_RVXF_1 | 316 | 323 | PF00149 | 0.400 |
DOC_SPAK_OSR1_1 | 367 | 371 | PF12202 | 0.517 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.410 |
DOC_USP7_MATH_1 | 82 | 86 | PF00917 | 0.477 |
DOC_USP7_MATH_2 | 292 | 298 | PF00917 | 0.553 |
DOC_WW_Pin1_4 | 226 | 231 | PF00397 | 0.400 |
LIG_14-3-3_CanoR_1 | 116 | 122 | PF00244 | 0.513 |
LIG_14-3-3_CanoR_1 | 214 | 223 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 235 | 240 | PF00244 | 0.400 |
LIG_14-3-3_CanoR_1 | 367 | 377 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 386 | 394 | PF00244 | 0.401 |
LIG_14-3-3_CanoR_1 | 414 | 422 | PF00244 | 0.491 |
LIG_Actin_WH2_2 | 219 | 237 | PF00022 | 0.537 |
LIG_BIR_III_2 | 289 | 293 | PF00653 | 0.581 |
LIG_BIR_III_4 | 267 | 271 | PF00653 | 0.400 |
LIG_eIF4E_1 | 207 | 213 | PF01652 | 0.483 |
LIG_FHA_1 | 130 | 136 | PF00498 | 0.508 |
LIG_FHA_1 | 251 | 257 | PF00498 | 0.565 |
LIG_FHA_2 | 118 | 124 | PF00498 | 0.500 |
LIG_FHA_2 | 253 | 259 | PF00498 | 0.581 |
LIG_FHA_2 | 337 | 343 | PF00498 | 0.491 |
LIG_FHA_2 | 371 | 377 | PF00498 | 0.481 |
LIG_LIR_Apic_2 | 139 | 144 | PF02991 | 0.562 |
LIG_LIR_Gen_1 | 2 | 11 | PF02991 | 0.532 |
LIG_LIR_Gen_1 | 319 | 327 | PF02991 | 0.505 |
LIG_LIR_Gen_1 | 395 | 405 | PF02991 | 0.549 |
LIG_LIR_Gen_1 | 78 | 88 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 2 | 8 | PF02991 | 0.536 |
LIG_LIR_Nem_3 | 319 | 325 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 341 | 347 | PF02991 | 0.580 |
LIG_LIR_Nem_3 | 395 | 400 | PF02991 | 0.549 |
LIG_LIR_Nem_3 | 58 | 63 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 78 | 83 | PF02991 | 0.439 |
LIG_PTB_Apo_2 | 348 | 355 | PF02174 | 0.497 |
LIG_PTB_Phospho_1 | 348 | 354 | PF10480 | 0.497 |
LIG_SH2_CRK | 174 | 178 | PF00017 | 0.400 |
LIG_SH2_CRK | 344 | 348 | PF00017 | 0.400 |
LIG_SH2_CRK | 397 | 401 | PF00017 | 0.400 |
LIG_SH2_CRK | 80 | 84 | PF00017 | 0.523 |
LIG_SH2_NCK_1 | 80 | 84 | PF00017 | 0.499 |
LIG_SH2_PTP2 | 354 | 357 | PF00017 | 0.562 |
LIG_SH2_STAP1 | 131 | 135 | PF00017 | 0.540 |
LIG_SH2_STAP1 | 168 | 172 | PF00017 | 0.581 |
LIG_SH2_STAP1 | 361 | 365 | PF00017 | 0.566 |
LIG_SH2_STAP1 | 80 | 84 | PF00017 | 0.526 |
LIG_SH2_STAT5 | 131 | 134 | PF00017 | 0.549 |
LIG_SH2_STAT5 | 207 | 210 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 211 | 214 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 354 | 357 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 369 | 372 | PF00017 | 0.420 |
LIG_SH3_3 | 116 | 122 | PF00018 | 0.400 |
LIG_SH3_3 | 15 | 21 | PF00018 | 0.445 |
LIG_SH3_3 | 203 | 209 | PF00018 | 0.525 |
LIG_SH3_3 | 242 | 248 | PF00018 | 0.535 |
LIG_SH3_3 | 268 | 274 | PF00018 | 0.552 |
LIG_SH3_5 | 357 | 361 | PF00018 | 0.581 |
LIG_SUMO_SIM_anti_2 | 376 | 381 | PF11976 | 0.487 |
LIG_SUMO_SIM_par_1 | 252 | 258 | PF11976 | 0.581 |
LIG_SUMO_SIM_par_1 | 323 | 331 | PF11976 | 0.400 |
LIG_SUMO_SIM_par_1 | 378 | 384 | PF11976 | 0.502 |
LIG_SUMO_SIM_par_1 | 423 | 428 | PF11976 | 0.501 |
LIG_TRAF2_1 | 121 | 124 | PF00917 | 0.400 |
LIG_TRAF2_1 | 180 | 183 | PF00917 | 0.400 |
LIG_TRAF2_1 | 255 | 258 | PF00917 | 0.581 |
LIG_TRAF2_1 | 339 | 342 | PF00917 | 0.554 |
LIG_TYR_ITIM | 172 | 177 | PF00017 | 0.581 |
LIG_UBA3_1 | 6 | 13 | PF00899 | 0.474 |
MOD_CK1_1 | 196 | 202 | PF00069 | 0.569 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.670 |
MOD_CK1_1 | 334 | 340 | PF00069 | 0.586 |
MOD_CK1_1 | 34 | 40 | PF00069 | 0.572 |
MOD_CK1_1 | 390 | 396 | PF00069 | 0.516 |
MOD_CK1_1 | 398 | 404 | PF00069 | 0.497 |
MOD_CK1_1 | 99 | 105 | PF00069 | 0.581 |
MOD_CK2_1 | 117 | 123 | PF00069 | 0.400 |
MOD_CK2_1 | 177 | 183 | PF00069 | 0.521 |
MOD_CK2_1 | 252 | 258 | PF00069 | 0.560 |
MOD_CK2_1 | 336 | 342 | PF00069 | 0.472 |
MOD_CK2_1 | 385 | 391 | PF00069 | 0.468 |
MOD_Cter_Amidation | 68 | 71 | PF01082 | 0.523 |
MOD_GlcNHglycan | 138 | 141 | PF01048 | 0.376 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.383 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.385 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.346 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.585 |
MOD_GlcNHglycan | 267 | 271 | PF01048 | 0.227 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.449 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.480 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.539 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.654 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.518 |
MOD_LATS_1 | 441 | 447 | PF00433 | 0.466 |
MOD_N-GLC_1 | 105 | 110 | PF02516 | 0.342 |
MOD_N-GLC_1 | 215 | 220 | PF02516 | 0.200 |
MOD_N-GLC_1 | 443 | 448 | PF02516 | 0.482 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.515 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.529 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.484 |
MOD_NEK2_1 | 368 | 373 | PF00069 | 0.476 |
MOD_PIKK_1 | 38 | 44 | PF00454 | 0.586 |
MOD_PKA_2 | 177 | 183 | PF00069 | 0.436 |
MOD_PKA_2 | 34 | 40 | PF00069 | 0.524 |
MOD_PKA_2 | 385 | 391 | PF00069 | 0.558 |
MOD_PKA_2 | 413 | 419 | PF00069 | 0.573 |
MOD_Plk_1 | 1 | 7 | PF00069 | 0.565 |
MOD_Plk_1 | 129 | 135 | PF00069 | 0.565 |
MOD_Plk_1 | 375 | 381 | PF00069 | 0.476 |
MOD_Plk_1 | 390 | 396 | PF00069 | 0.476 |
MOD_Plk_1 | 99 | 105 | PF00069 | 0.542 |
MOD_Plk_2-3 | 252 | 258 | PF00069 | 0.400 |
MOD_Plk_4 | 1 | 7 | PF00069 | 0.508 |
MOD_Plk_4 | 375 | 381 | PF00069 | 0.482 |
MOD_Plk_4 | 395 | 401 | PF00069 | 0.506 |
MOD_Plk_4 | 82 | 88 | PF00069 | 0.504 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.484 |
MOD_Plk_4 | 99 | 105 | PF00069 | 0.520 |
MOD_ProDKin_1 | 226 | 232 | PF00069 | 0.400 |
MOD_SUMO_rev_2 | 130 | 137 | PF00179 | 0.505 |
MOD_SUMO_rev_2 | 426 | 431 | PF00179 | 0.518 |
TRG_ENDOCYTIC_2 | 168 | 171 | PF00928 | 0.537 |
TRG_ENDOCYTIC_2 | 174 | 177 | PF00928 | 0.537 |
TRG_ENDOCYTIC_2 | 344 | 347 | PF00928 | 0.400 |
TRG_ENDOCYTIC_2 | 397 | 400 | PF00928 | 0.400 |
TRG_ENDOCYTIC_2 | 60 | 63 | PF00928 | 0.496 |
TRG_ENDOCYTIC_2 | 80 | 83 | PF00928 | 0.458 |
TRG_ER_diArg_1 | 46 | 49 | PF00400 | 0.484 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDW9 | Leptomonas seymouri | 54% | 100% |
A0A0S4KLU4 | Bodo saltans | 26% | 92% |
A0A1X0PAD2 | Trypanosomatidae | 31% | 100% |
A0A3Q8IEN4 | Leishmania donovani | 75% | 100% |
A0A3R7K0N1 | Trypanosoma rangeli | 30% | 99% |
A4IAD7 | Leishmania infantum | 75% | 100% |
C9ZLV8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9B5G1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 74% | 100% |
Q4Q2H4 | Leishmania major | 75% | 100% |
V5B6A7 | Trypanosoma cruzi | 31% | 90% |