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:0005886 | plasma membrane | 3 | 1 |
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HNP5
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:0006629 | lipid metabolic process | 3 | 1 |
GO:0006644 | phospholipid metabolic process | 4 | 1 |
GO:0006650 | glycerophospholipid metabolic process | 5 | 1 |
GO:0006661 | phosphatidylinositol biosynthetic process | 6 | 1 |
GO:0008610 | lipid biosynthetic process | 4 | 1 |
GO:0008654 | phospholipid biosynthetic process | 5 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0019637 | organophosphate metabolic process | 3 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044255 | cellular lipid metabolic process | 3 | 1 |
GO:0045017 | glycerolipid biosynthetic process | 4 | 1 |
GO:0046474 | glycerophospholipid biosynthetic process | 5 | 1 |
GO:0046486 | glycerolipid metabolic process | 4 | 1 |
GO:0046488 | phosphatidylinositol metabolic process | 6 | 1 |
GO:0046854 | phosphatidylinositol phosphate biosynthetic process | 7 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090407 | organophosphate biosynthetic process | 4 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 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:0016307 | phosphatidylinositol phosphate kinase activity | 5 | 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: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 |
GO:0016308 | 1-phosphatidylinositol-4-phosphate 5-kinase activity | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 182 | 184 | PF00675 | 0.271 |
CLV_NRD_NRD_1 | 226 | 228 | PF00675 | 0.277 |
CLV_NRD_NRD_1 | 292 | 294 | PF00675 | 0.350 |
CLV_NRD_NRD_1 | 436 | 438 | PF00675 | 0.255 |
CLV_PCSK_KEX2_1 | 226 | 228 | PF00082 | 0.259 |
CLV_PCSK_KEX2_1 | 241 | 243 | PF00082 | 0.336 |
CLV_PCSK_KEX2_1 | 294 | 296 | PF00082 | 0.383 |
CLV_PCSK_KEX2_1 | 436 | 438 | PF00082 | 0.305 |
CLV_PCSK_KEX2_1 | 79 | 81 | PF00082 | 0.429 |
CLV_PCSK_PC1ET2_1 | 241 | 243 | PF00082 | 0.219 |
CLV_PCSK_PC1ET2_1 | 294 | 296 | PF00082 | 0.387 |
CLV_PCSK_PC1ET2_1 | 79 | 81 | PF00082 | 0.441 |
CLV_PCSK_SKI1_1 | 12 | 16 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 150 | 154 | PF00082 | 0.399 |
CLV_PCSK_SKI1_1 | 247 | 251 | PF00082 | 0.206 |
CLV_PCSK_SKI1_1 | 266 | 270 | PF00082 | 0.238 |
CLV_PCSK_SKI1_1 | 280 | 284 | PF00082 | 0.244 |
CLV_PCSK_SKI1_1 | 294 | 298 | PF00082 | 0.242 |
CLV_PCSK_SKI1_1 | 417 | 421 | PF00082 | 0.278 |
CLV_PCSK_SKI1_1 | 436 | 440 | PF00082 | 0.403 |
CLV_PCSK_SKI1_1 | 56 | 60 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 79 | 83 | PF00082 | 0.472 |
DEG_APCC_DBOX_1 | 149 | 157 | PF00400 | 0.230 |
DOC_CYCLIN_RxL_1 | 291 | 298 | PF00134 | 0.275 |
DOC_MAPK_gen_1 | 183 | 192 | PF00069 | 0.175 |
DOC_MAPK_gen_1 | 226 | 233 | PF00069 | 0.280 |
DOC_MAPK_gen_1 | 77 | 85 | PF00069 | 0.539 |
DOC_MAPK_HePTP_8 | 170 | 182 | PF00069 | 0.276 |
DOC_MAPK_MEF2A_6 | 173 | 182 | PF00069 | 0.251 |
DOC_MAPK_MEF2A_6 | 226 | 235 | PF00069 | 0.165 |
DOC_MAPK_MEF2A_6 | 77 | 85 | PF00069 | 0.560 |
DOC_MAPK_NFAT4_5 | 173 | 181 | PF00069 | 0.247 |
DOC_PP2B_LxvP_1 | 14 | 17 | PF13499 | 0.283 |
DOC_PP2B_LxvP_1 | 69 | 72 | PF13499 | 0.385 |
DOC_PP4_FxxP_1 | 286 | 289 | PF00568 | 0.418 |
DOC_USP7_MATH_1 | 197 | 201 | PF00917 | 0.165 |
DOC_USP7_MATH_1 | 215 | 219 | PF00917 | 0.182 |
DOC_USP7_MATH_1 | 349 | 353 | PF00917 | 0.324 |
DOC_USP7_MATH_1 | 363 | 367 | PF00917 | 0.229 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.522 |
DOC_USP7_MATH_1 | 447 | 451 | PF00917 | 0.325 |
DOC_USP7_MATH_1 | 52 | 56 | PF00917 | 0.358 |
DOC_USP7_UBL2_3 | 205 | 209 | PF12436 | 0.257 |
DOC_WW_Pin1_4 | 270 | 275 | PF00397 | 0.165 |
DOC_WW_Pin1_4 | 375 | 380 | PF00397 | 0.246 |
LIG_14-3-3_CanoR_1 | 12 | 17 | PF00244 | 0.609 |
LIG_14-3-3_CanoR_1 | 24 | 28 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 436 | 442 | PF00244 | 0.388 |
LIG_14-3-3_CanoR_1 | 48 | 52 | PF00244 | 0.293 |
LIG_14-3-3_CanoR_1 | 68 | 72 | PF00244 | 0.374 |
LIG_Actin_WH2_2 | 16 | 34 | PF00022 | 0.364 |
LIG_AP2alpha_1 | 192 | 196 | PF02296 | 0.233 |
LIG_BRCT_BRCA1_1 | 126 | 130 | PF00533 | 0.391 |
LIG_DLG_GKlike_1 | 437 | 444 | PF00625 | 0.387 |
LIG_FHA_1 | 141 | 147 | PF00498 | 0.395 |
LIG_FHA_1 | 440 | 446 | PF00498 | 0.257 |
LIG_FHA_2 | 274 | 280 | PF00498 | 0.242 |
LIG_FHA_2 | 320 | 326 | PF00498 | 0.271 |
LIG_FHA_2 | 376 | 382 | PF00498 | 0.387 |
LIG_LIR_Apic_2 | 109 | 114 | PF02991 | 0.335 |
LIG_LIR_Apic_2 | 283 | 289 | PF02991 | 0.387 |
LIG_LIR_Gen_1 | 303 | 312 | PF02991 | 0.278 |
LIG_LIR_Gen_1 | 314 | 323 | PF02991 | 0.242 |
LIG_LIR_Gen_1 | 352 | 362 | PF02991 | 0.165 |
LIG_LIR_Gen_1 | 439 | 449 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 303 | 307 | PF02991 | 0.292 |
LIG_LIR_Nem_3 | 314 | 318 | PF02991 | 0.259 |
LIG_LIR_Nem_3 | 352 | 357 | PF02991 | 0.165 |
LIG_LIR_Nem_3 | 393 | 399 | PF02991 | 0.257 |
LIG_LIR_Nem_3 | 439 | 444 | PF02991 | 0.301 |
LIG_NRBOX | 296 | 302 | PF00104 | 0.165 |
LIG_NRP_CendR_1 | 454 | 456 | PF00754 | 0.467 |
LIG_Pex14_2 | 107 | 111 | PF04695 | 0.306 |
LIG_Pex14_2 | 192 | 196 | PF04695 | 0.245 |
LIG_Pex14_2 | 415 | 419 | PF04695 | 0.166 |
LIG_PTB_Apo_2 | 218 | 225 | PF02174 | 0.165 |
LIG_REV1ctd_RIR_1 | 128 | 137 | PF16727 | 0.230 |
LIG_REV1ctd_RIR_1 | 413 | 421 | PF16727 | 0.301 |
LIG_SH2_CRK | 175 | 179 | PF00017 | 0.389 |
LIG_SH2_CRK | 304 | 308 | PF00017 | 0.336 |
LIG_SH2_CRK | 315 | 319 | PF00017 | 0.242 |
LIG_SH2_PTP2 | 396 | 399 | PF00017 | 0.242 |
LIG_SH2_STAP1 | 315 | 319 | PF00017 | 0.242 |
LIG_SH2_STAP1 | 434 | 438 | PF00017 | 0.303 |
LIG_SH2_STAT5 | 188 | 191 | PF00017 | 0.269 |
LIG_SH2_STAT5 | 396 | 399 | PF00017 | 0.242 |
LIG_SH2_STAT5 | 406 | 409 | PF00017 | 0.242 |
LIG_SH3_3 | 374 | 380 | PF00018 | 0.165 |
LIG_SUMO_SIM_par_1 | 142 | 148 | PF11976 | 0.285 |
LIG_SUMO_SIM_par_1 | 398 | 404 | PF11976 | 0.387 |
LIG_TRAF2_1 | 145 | 148 | PF00917 | 0.336 |
LIG_TRAF2_1 | 449 | 452 | PF00917 | 0.373 |
LIG_TYR_ITIM | 394 | 399 | PF00017 | 0.229 |
LIG_WRC_WIRS_1 | 416 | 421 | PF05994 | 0.191 |
LIG_WRC_WIRS_1 | 438 | 443 | PF05994 | 0.387 |
LIG_WRC_WIRS_1 | 92 | 97 | PF05994 | 0.416 |
LIG_WW_1 | 430 | 433 | PF00397 | 0.165 |
MOD_CK1_1 | 273 | 279 | PF00069 | 0.165 |
MOD_CK1_1 | 350 | 356 | PF00069 | 0.170 |
MOD_CK1_1 | 366 | 372 | PF00069 | 0.180 |
MOD_CK1_1 | 450 | 456 | PF00069 | 0.482 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.446 |
MOD_CK2_1 | 109 | 115 | PF00069 | 0.406 |
MOD_CK2_1 | 142 | 148 | PF00069 | 0.283 |
MOD_CK2_1 | 319 | 325 | PF00069 | 0.271 |
MOD_CK2_1 | 350 | 356 | PF00069 | 0.411 |
MOD_CK2_1 | 375 | 381 | PF00069 | 0.422 |
MOD_CK2_1 | 385 | 391 | PF00069 | 0.329 |
MOD_CK2_1 | 437 | 443 | PF00069 | 0.349 |
MOD_CK2_1 | 47 | 53 | PF00069 | 0.495 |
MOD_Cter_Amidation | 77 | 80 | PF01082 | 0.339 |
MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.357 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.257 |
MOD_GlcNHglycan | 342 | 345 | PF01048 | 0.338 |
MOD_GlcNHglycan | 349 | 352 | PF01048 | 0.439 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.437 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.306 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.404 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.562 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.507 |
MOD_LATS_1 | 278 | 284 | PF00433 | 0.387 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.242 |
MOD_NEK2_1 | 140 | 145 | PF00069 | 0.242 |
MOD_NEK2_1 | 178 | 183 | PF00069 | 0.306 |
MOD_NEK2_1 | 306 | 311 | PF00069 | 0.326 |
MOD_NEK2_1 | 313 | 318 | PF00069 | 0.288 |
MOD_NEK2_1 | 340 | 345 | PF00069 | 0.186 |
MOD_NEK2_1 | 415 | 420 | PF00069 | 0.283 |
MOD_NEK2_1 | 425 | 430 | PF00069 | 0.257 |
MOD_NEK2_2 | 215 | 220 | PF00069 | 0.165 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.536 |
MOD_PIKK_1 | 124 | 130 | PF00454 | 0.387 |
MOD_PIKK_1 | 38 | 44 | PF00454 | 0.556 |
MOD_PK_1 | 142 | 148 | PF00069 | 0.285 |
MOD_PKA_1 | 226 | 232 | PF00069 | 0.290 |
MOD_PKA_1 | 371 | 377 | PF00069 | 0.285 |
MOD_PKA_1 | 436 | 442 | PF00069 | 0.247 |
MOD_PKA_2 | 226 | 232 | PF00069 | 0.222 |
MOD_PKA_2 | 23 | 29 | PF00069 | 0.493 |
MOD_PKA_2 | 338 | 344 | PF00069 | 0.208 |
MOD_PKA_2 | 436 | 442 | PF00069 | 0.275 |
MOD_PKA_2 | 47 | 53 | PF00069 | 0.312 |
MOD_PKA_2 | 67 | 73 | PF00069 | 0.434 |
MOD_Plk_1 | 109 | 115 | PF00069 | 0.388 |
MOD_Plk_1 | 280 | 286 | PF00069 | 0.241 |
MOD_Plk_1 | 313 | 319 | PF00069 | 0.257 |
MOD_Plk_2-3 | 109 | 115 | PF00069 | 0.399 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.267 |
MOD_Plk_4 | 197 | 203 | PF00069 | 0.379 |
MOD_Plk_4 | 313 | 319 | PF00069 | 0.254 |
MOD_Plk_4 | 415 | 421 | PF00069 | 0.257 |
MOD_ProDKin_1 | 270 | 276 | PF00069 | 0.165 |
MOD_ProDKin_1 | 375 | 381 | PF00069 | 0.246 |
MOD_SUMO_rev_2 | 261 | 271 | PF00179 | 0.165 |
MOD_SUMO_rev_2 | 365 | 374 | PF00179 | 0.430 |
TRG_DiLeu_BaEn_1 | 148 | 153 | PF01217 | 0.242 |
TRG_DiLeu_BaLyEn_6 | 292 | 297 | PF01217 | 0.271 |
TRG_ENDOCYTIC_2 | 175 | 178 | PF00928 | 0.347 |
TRG_ENDOCYTIC_2 | 304 | 307 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 315 | 318 | PF00928 | 0.262 |
TRG_ENDOCYTIC_2 | 396 | 399 | PF00928 | 0.242 |
TRG_ER_diArg_1 | 225 | 227 | PF00400 | 0.233 |
TRG_ER_diArg_1 | 293 | 296 | PF00400 | 0.387 |
TRG_ER_diArg_1 | 436 | 438 | PF00400 | 0.255 |
TRG_NLS_Bipartite_1 | 226 | 244 | PF00514 | 0.165 |
TRG_NLS_MonoExtC_3 | 292 | 298 | PF00514 | 0.307 |
TRG_NLS_MonoExtN_4 | 77 | 83 | PF00514 | 0.304 |
TRG_Pf-PMV_PEXEL_1 | 150 | 154 | PF00026 | 0.165 |
TRG_Pf-PMV_PEXEL_1 | 294 | 298 | PF00026 | 0.389 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCT9 | Leptomonas seymouri | 23% | 83% |
A0A0N1PE70 | Leptomonas seymouri | 55% | 100% |
A0A0S4IZA7 | Bodo saltans | 24% | 99% |
A0A0S4JRR3 | Bodo saltans | 41% | 98% |
A0A1X0P9B0 | Trypanosomatidae | 47% | 100% |
A0A1X0PB79 | Trypanosomatidae | 23% | 96% |
A0A381MTN1 | Leishmania infantum | 22% | 84% |
A0A3Q8ILB5 | Leishmania donovani | 22% | 84% |
A0A3R7KQW9 | Trypanosoma rangeli | 45% | 100% |
A0A3S7XA92 | Leishmania donovani | 68% | 100% |
A0A422N247 | Trypanosoma rangeli | 23% | 96% |
A4HB28 | Leishmania braziliensis | 22% | 100% |
A4ICV0 | Leishmania infantum | 68% | 100% |
C9ZM20 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 95% |
D0A2K2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
D3ZSI8 | Rattus norvegicus | 24% | 84% |
E9ASF4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 64% | 100% |
E9B598 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 22% | 84% |
O13010 | Sus scrofa | 25% | 100% |
O60331 | Homo sapiens | 25% | 68% |
O70161 | Mus musculus | 24% | 69% |
O70172 | Mus musculus | 25% | 100% |
O88377 | Rattus norvegicus | 24% | 100% |
P48426 | Homo sapiens | 25% | 100% |
P70182 | Mus musculus | 25% | 84% |
P78356 | Homo sapiens | 24% | 100% |
Q0P5F7 | Bos taurus | 26% | 100% |
Q17QS4 | Bos taurus | 25% | 100% |
Q4Q241 | Leishmania major | 66% | 100% |
Q4Q2N5 | Leishmania major | 22% | 84% |
Q5F356 | Gallus gallus | 25% | 100% |
Q5I6B8 | Rattus norvegicus | 24% | 66% |
Q5PQ01 | Xenopus laevis | 26% | 100% |
Q5T9C9 | Homo sapiens | 26% | 100% |
Q6GL14 | Xenopus tropicalis | 26% | 100% |
Q6IQE1 | Danio rerio | 24% | 100% |
Q80XI4 | Mus musculus | 24% | 100% |
Q8TBX8 | Homo sapiens | 26% | 100% |
Q91XU3 | Mus musculus | 25% | 100% |
Q99755 | Homo sapiens | 25% | 81% |
Q9R0I8 | Rattus norvegicus | 25% | 100% |
V5BA13 | Trypanosoma cruzi | 47% | 100% |
V5BV28 | Trypanosoma cruzi | 24% | 96% |