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: 1, no: 11 |
NetGPI | no | yes: 0, no: 12 |
Related structures:
AlphaFold database: A4HF96
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 13 |
GO:0006793 | phosphorus metabolic process | 3 | 13 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 13 |
GO:0006807 | nitrogen compound metabolic process | 2 | 13 |
GO:0008152 | metabolic process | 1 | 13 |
GO:0009987 | cellular process | 1 | 13 |
GO:0016310 | phosphorylation | 5 | 13 |
GO:0019538 | protein metabolic process | 3 | 13 |
GO:0036211 | protein modification process | 4 | 13 |
GO:0043170 | macromolecule metabolic process | 3 | 13 |
GO:0043412 | macromolecule modification | 4 | 13 |
GO:0044237 | cellular metabolic process | 2 | 13 |
GO:0044238 | primary metabolic process | 2 | 13 |
GO:0071704 | organic substance metabolic process | 2 | 13 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 13 |
GO:0003824 | catalytic activity | 1 | 13 |
GO:0004672 | protein kinase activity | 3 | 13 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 11 |
GO:0005488 | binding | 1 | 13 |
GO:0005524 | ATP binding | 5 | 13 |
GO:0016301 | kinase activity | 4 | 13 |
GO:0016740 | transferase activity | 2 | 13 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 13 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 13 |
GO:0017076 | purine nucleotide binding | 4 | 13 |
GO:0030554 | adenyl nucleotide binding | 5 | 13 |
GO:0032553 | ribonucleotide binding | 3 | 13 |
GO:0032555 | purine ribonucleotide binding | 4 | 13 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 13 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 13 |
GO:0036094 | small molecule binding | 2 | 13 |
GO:0043167 | ion binding | 2 | 13 |
GO:0043168 | anion binding | 3 | 13 |
GO:0043169 | cation binding | 3 | 13 |
GO:0046872 | metal ion binding | 4 | 13 |
GO:0097159 | organic cyclic compound binding | 2 | 13 |
GO:0097367 | carbohydrate derivative binding | 2 | 13 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 13 |
GO:1901265 | nucleoside phosphate binding | 3 | 13 |
GO:1901363 | heterocyclic compound binding | 2 | 13 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 166 | 168 | PF00675 | 0.190 |
CLV_NRD_NRD_1 | 228 | 230 | PF00675 | 0.353 |
CLV_NRD_NRD_1 | 29 | 31 | PF00675 | 0.344 |
CLV_NRD_NRD_1 | 33 | 35 | PF00675 | 0.342 |
CLV_NRD_NRD_1 | 370 | 372 | PF00675 | 0.341 |
CLV_NRD_NRD_1 | 68 | 70 | PF00675 | 0.267 |
CLV_PCSK_KEX2_1 | 165 | 167 | PF00082 | 0.306 |
CLV_PCSK_KEX2_1 | 175 | 177 | PF00082 | 0.328 |
CLV_PCSK_KEX2_1 | 228 | 230 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 29 | 31 | PF00082 | 0.380 |
CLV_PCSK_KEX2_1 | 33 | 35 | PF00082 | 0.387 |
CLV_PCSK_KEX2_1 | 370 | 372 | PF00082 | 0.344 |
CLV_PCSK_KEX2_1 | 59 | 61 | PF00082 | 0.431 |
CLV_PCSK_PC1ET2_1 | 175 | 177 | PF00082 | 0.257 |
CLV_PCSK_PC1ET2_1 | 59 | 61 | PF00082 | 0.289 |
CLV_PCSK_PC7_1 | 29 | 35 | PF00082 | 0.400 |
CLV_PCSK_SKI1_1 | 106 | 110 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 160 | 164 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 167 | 171 | PF00082 | 0.263 |
CLV_PCSK_SKI1_1 | 269 | 273 | PF00082 | 0.249 |
CLV_PCSK_SKI1_1 | 431 | 435 | PF00082 | 0.582 |
DEG_APCC_DBOX_1 | 166 | 174 | PF00400 | 0.278 |
DEG_APCC_DBOX_1 | 211 | 219 | PF00400 | 0.400 |
DEG_APCC_KENBOX_2 | 408 | 412 | PF00400 | 0.330 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.666 |
DEG_SPOP_SBC_1 | 465 | 469 | PF00917 | 0.376 |
DOC_CKS1_1 | 10 | 15 | PF01111 | 0.530 |
DOC_CKS1_1 | 102 | 107 | PF01111 | 0.513 |
DOC_CKS1_1 | 282 | 287 | PF01111 | 0.400 |
DOC_MAPK_gen_1 | 269 | 278 | PF00069 | 0.249 |
DOC_MAPK_MEF2A_6 | 212 | 219 | PF00069 | 0.400 |
DOC_USP7_MATH_1 | 356 | 360 | PF00917 | 0.330 |
DOC_USP7_UBL2_3 | 171 | 175 | PF12436 | 0.252 |
DOC_WW_Pin1_4 | 101 | 106 | PF00397 | 0.531 |
DOC_WW_Pin1_4 | 281 | 286 | PF00397 | 0.400 |
DOC_WW_Pin1_4 | 395 | 400 | PF00397 | 0.202 |
DOC_WW_Pin1_4 | 415 | 420 | PF00397 | 0.235 |
DOC_WW_Pin1_4 | 9 | 14 | PF00397 | 0.539 |
LIG_14-3-3_CanoR_1 | 160 | 169 | PF00244 | 0.452 |
LIG_14-3-3_CanoR_1 | 176 | 182 | PF00244 | 0.259 |
LIG_14-3-3_CanoR_1 | 81 | 85 | PF00244 | 0.554 |
LIG_14-3-3_CterR_2 | 482 | 485 | PF00244 | 0.419 |
LIG_APCC_ABBAyCdc20_2 | 264 | 270 | PF00400 | 0.249 |
LIG_BRCT_BRCA1_1 | 358 | 362 | PF00533 | 0.330 |
LIG_BRCT_BRCA1_2 | 358 | 364 | PF00533 | 0.330 |
LIG_FHA_1 | 107 | 113 | PF00498 | 0.496 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.309 |
LIG_FHA_1 | 19 | 25 | PF00498 | 0.318 |
LIG_FHA_1 | 244 | 250 | PF00498 | 0.286 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.357 |
LIG_FHA_1 | 416 | 422 | PF00498 | 0.411 |
LIG_FHA_1 | 5 | 11 | PF00498 | 0.683 |
LIG_FHA_2 | 159 | 165 | PF00498 | 0.167 |
LIG_FHA_2 | 209 | 215 | PF00498 | 0.331 |
LIG_FHA_2 | 437 | 443 | PF00498 | 0.644 |
LIG_LIR_Apic_2 | 279 | 285 | PF02991 | 0.400 |
LIG_LIR_Apic_2 | 309 | 315 | PF02991 | 0.249 |
LIG_LIR_Gen_1 | 114 | 124 | PF02991 | 0.339 |
LIG_LIR_Gen_1 | 359 | 369 | PF02991 | 0.331 |
LIG_LIR_Gen_1 | 404 | 413 | PF02991 | 0.437 |
LIG_LIR_Gen_1 | 442 | 451 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 150 | 154 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 300 | 306 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 404 | 408 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 442 | 446 | PF02991 | 0.501 |
LIG_MAD2 | 192 | 200 | PF02301 | 0.317 |
LIG_Pex14_1 | 472 | 476 | PF04695 | 0.613 |
LIG_Pex14_2 | 151 | 155 | PF04695 | 0.330 |
LIG_Pex14_2 | 35 | 39 | PF04695 | 0.322 |
LIG_Pex14_2 | 80 | 84 | PF04695 | 0.512 |
LIG_SH2_CRK | 130 | 134 | PF00017 | 0.477 |
LIG_SH2_CRK | 282 | 286 | PF00017 | 0.368 |
LIG_SH2_CRK | 405 | 409 | PF00017 | 0.330 |
LIG_SH2_NCK_1 | 312 | 316 | PF00017 | 0.355 |
LIG_SH2_NCK_1 | 397 | 401 | PF00017 | 0.330 |
LIG_SH2_STAP1 | 181 | 185 | PF00017 | 0.442 |
LIG_SH2_STAT3 | 63 | 66 | PF00017 | 0.330 |
LIG_SH2_STAT5 | 102 | 105 | PF00017 | 0.535 |
LIG_SH2_STAT5 | 116 | 119 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 181 | 184 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 259 | 262 | PF00017 | 0.249 |
LIG_SH2_STAT5 | 304 | 307 | PF00017 | 0.298 |
LIG_SH2_STAT5 | 349 | 352 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 476 | 479 | PF00017 | 0.625 |
LIG_SH2_STAT5 | 52 | 55 | PF00017 | 0.390 |
LIG_SH3_3 | 194 | 200 | PF00018 | 0.330 |
LIG_SH3_3 | 459 | 465 | PF00018 | 0.667 |
LIG_SUMO_SIM_anti_2 | 213 | 220 | PF11976 | 0.322 |
LIG_SUMO_SIM_par_1 | 213 | 220 | PF11976 | 0.265 |
LIG_TRAF2_2 | 399 | 404 | PF00917 | 0.330 |
LIG_TYR_ITIM | 346 | 351 | PF00017 | 0.262 |
LIG_UBA3_1 | 169 | 175 | PF00899 | 0.330 |
LIG_WRC_WIRS_1 | 137 | 142 | PF05994 | 0.382 |
MOD_CDK_SPK_2 | 101 | 106 | PF00069 | 0.520 |
MOD_CDK_SPxxK_3 | 395 | 402 | PF00069 | 0.292 |
MOD_CDK_SPxxK_3 | 415 | 422 | PF00069 | 0.234 |
MOD_CK1_1 | 114 | 120 | PF00069 | 0.349 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.292 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.482 |
MOD_CK2_1 | 436 | 442 | PF00069 | 0.609 |
MOD_Cter_Amidation | 27 | 30 | PF01082 | 0.400 |
MOD_Cter_Amidation | 31 | 34 | PF01082 | 0.400 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.400 |
MOD_GlcNHglycan | 351 | 354 | PF01048 | 0.298 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.167 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.278 |
MOD_GSK3_1 | 442 | 449 | PF00069 | 0.651 |
MOD_GSK3_1 | 478 | 485 | PF00069 | 0.622 |
MOD_N-GLC_1 | 177 | 182 | PF02516 | 0.400 |
MOD_N-GLC_2 | 72 | 74 | PF02516 | 0.262 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.718 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.444 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.382 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.331 |
MOD_NEK2_1 | 466 | 471 | PF00069 | 0.493 |
MOD_NEK2_1 | 80 | 85 | PF00069 | 0.540 |
MOD_NEK2_2 | 331 | 336 | PF00069 | 0.400 |
MOD_PIKK_1 | 466 | 472 | PF00454 | 0.381 |
MOD_PKA_2 | 147 | 153 | PF00069 | 0.400 |
MOD_PKA_2 | 4 | 10 | PF00069 | 0.436 |
MOD_PKA_2 | 478 | 484 | PF00069 | 0.670 |
MOD_PKA_2 | 80 | 86 | PF00069 | 0.585 |
MOD_Plk_1 | 177 | 183 | PF00069 | 0.395 |
MOD_Plk_1 | 18 | 24 | PF00069 | 0.173 |
MOD_Plk_2-3 | 442 | 448 | PF00069 | 0.592 |
MOD_Plk_4 | 114 | 120 | PF00069 | 0.533 |
MOD_Plk_4 | 136 | 142 | PF00069 | 0.329 |
MOD_Plk_4 | 150 | 156 | PF00069 | 0.249 |
MOD_ProDKin_1 | 101 | 107 | PF00069 | 0.529 |
MOD_ProDKin_1 | 281 | 287 | PF00069 | 0.400 |
MOD_ProDKin_1 | 395 | 401 | PF00069 | 0.202 |
MOD_ProDKin_1 | 415 | 421 | PF00069 | 0.229 |
MOD_ProDKin_1 | 9 | 15 | PF00069 | 0.530 |
MOD_SUMO_for_1 | 155 | 158 | PF00179 | 0.330 |
TRG_DiLeu_BaEn_1 | 20 | 25 | PF01217 | 0.167 |
TRG_DiLeu_BaEn_1 | 459 | 464 | PF01217 | 0.555 |
TRG_DiLeu_BaLyEn_6 | 428 | 433 | PF01217 | 0.556 |
TRG_ENDOCYTIC_2 | 116 | 119 | PF00928 | 0.435 |
TRG_ENDOCYTIC_2 | 130 | 133 | PF00928 | 0.341 |
TRG_ENDOCYTIC_2 | 348 | 351 | PF00928 | 0.278 |
TRG_ENDOCYTIC_2 | 405 | 408 | PF00928 | 0.330 |
TRG_ER_diArg_1 | 165 | 167 | PF00400 | 0.184 |
TRG_ER_diArg_1 | 33 | 35 | PF00400 | 0.411 |
TRG_ER_diArg_1 | 369 | 371 | PF00400 | 0.343 |
TRG_Pf-PMV_PEXEL_1 | 388 | 392 | PF00026 | 0.322 |
TRG_Pf-PMV_PEXEL_1 | 431 | 435 | PF00026 | 0.491 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4J7 | Leptomonas seymouri | 23% | 100% |
A0A0N0P7K3 | Leptomonas seymouri | 65% | 100% |
A0A0S4IQ75 | Bodo saltans | 26% | 96% |
A0A0S4IRU8 | Bodo saltans | 24% | 100% |
A0A0S4J4B3 | Bodo saltans | 24% | 100% |
A0A0S4JH92 | Bodo saltans | 40% | 98% |
A0A0S4JQP0 | Bodo saltans | 41% | 99% |
A0A0S4KKJ1 | Bodo saltans | 23% | 77% |
A0A1X0P5U3 | Trypanosomatidae | 26% | 95% |
A0A1X0P834 | Trypanosomatidae | 45% | 100% |
A0A3Q8IHA5 | Leishmania donovani | 89% | 100% |
A0A3R7MPF2 | Trypanosoma rangeli | 26% | 75% |
A0A3R7RIN5 | Trypanosoma rangeli | 29% | 97% |
A0A3S5H5G0 | Leishmania donovani | 29% | 100% |
A0A422N3U8 | Trypanosoma rangeli | 27% | 67% |
A0A422P3P9 | Trypanosoma rangeli | 48% | 98% |
A4H459 | Leishmania braziliensis | 29% | 100% |
A4HCE6 | Leishmania braziliensis | 24% | 100% |
A4HSE2 | Leishmania infantum | 29% | 100% |
A4I2I8 | Leishmania infantum | 89% | 100% |
C9ZUU2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 74% |
C9ZX15 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 97% |
E9AKB7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9AKZ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9ALJ2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9AQF3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9AYN2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
P28867 | Mus musculus | 26% | 72% |
P31749 | Homo sapiens | 28% | 100% |
Q0VD22 | Bos taurus | 29% | 100% |
Q4Q8U0 | Leishmania major | 90% | 100% |
Q4QJJ0 | Leishmania major | 28% | 100% |
Q60823 | Mus musculus | 27% | 100% |
Q6IP76 | Xenopus laevis | 28% | 100% |
Q7ZX15 | Xenopus laevis | 28% | 100% |
Q8INB9 | Drosophila melanogaster | 28% | 79% |
Q9FZ36 | Arabidopsis thaliana | 24% | 75% |
Q9SN43 | Arabidopsis thaliana | 28% | 99% |
Q9ZSA2 | Arabidopsis thaliana | 27% | 91% |
V5BC57 | Trypanosoma cruzi | 47% | 98% |
V5C224 | Trypanosoma cruzi | 28% | 97% |