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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A4HW45
Term | Name | Level | Count |
---|---|---|---|
GO:0006793 | phosphorus metabolic process | 3 | 1 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016310 | phosphorylation | 5 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0016301 | kinase activity | 4 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 162 | 166 | PF00656 | 0.447 |
CLV_NRD_NRD_1 | 163 | 165 | PF00675 | 0.400 |
CLV_NRD_NRD_1 | 167 | 169 | PF00675 | 0.377 |
CLV_NRD_NRD_1 | 234 | 236 | PF00675 | 0.391 |
CLV_NRD_NRD_1 | 243 | 245 | PF00675 | 0.358 |
CLV_NRD_NRD_1 | 366 | 368 | PF00675 | 0.516 |
CLV_NRD_NRD_1 | 399 | 401 | PF00675 | 0.420 |
CLV_NRD_NRD_1 | 449 | 451 | PF00675 | 0.554 |
CLV_NRD_NRD_1 | 501 | 503 | PF00675 | 0.672 |
CLV_PCSK_FUR_1 | 397 | 401 | PF00082 | 0.441 |
CLV_PCSK_KEX2_1 | 163 | 165 | PF00082 | 0.400 |
CLV_PCSK_KEX2_1 | 234 | 236 | PF00082 | 0.355 |
CLV_PCSK_KEX2_1 | 366 | 368 | PF00082 | 0.466 |
CLV_PCSK_KEX2_1 | 377 | 379 | PF00082 | 0.424 |
CLV_PCSK_KEX2_1 | 399 | 401 | PF00082 | 0.439 |
CLV_PCSK_KEX2_1 | 501 | 503 | PF00082 | 0.672 |
CLV_PCSK_PC1ET2_1 | 377 | 379 | PF00082 | 0.480 |
CLV_PCSK_SKI1_1 | 164 | 168 | PF00082 | 0.370 |
CLV_PCSK_SKI1_1 | 272 | 276 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 374 | 378 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 382 | 386 | PF00082 | 0.419 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.589 |
DOC_AGCK_PIF_1 | 171 | 176 | PF00069 | 0.447 |
DOC_CKS1_1 | 144 | 149 | PF01111 | 0.447 |
DOC_CKS1_1 | 200 | 205 | PF01111 | 0.447 |
DOC_CYCLIN_yCln2_LP_2 | 282 | 288 | PF00134 | 0.419 |
DOC_CYCLIN_yCln2_LP_2 | 462 | 468 | PF00134 | 0.691 |
DOC_MAPK_gen_1 | 450 | 456 | PF00069 | 0.574 |
DOC_PP2B_LxvP_1 | 462 | 465 | PF13499 | 0.593 |
DOC_PP4_FxxP_1 | 144 | 147 | PF00568 | 0.408 |
DOC_PP4_FxxP_1 | 249 | 252 | PF00568 | 0.480 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.527 |
DOC_USP7_MATH_1 | 333 | 337 | PF00917 | 0.498 |
DOC_USP7_MATH_1 | 475 | 479 | PF00917 | 0.720 |
DOC_USP7_MATH_1 | 52 | 56 | PF00917 | 0.269 |
DOC_WD40_RPTOR_TOS_1 | 391 | 396 | PF00400 | 0.472 |
DOC_WW_Pin1_4 | 143 | 148 | PF00397 | 0.384 |
DOC_WW_Pin1_4 | 151 | 156 | PF00397 | 0.319 |
DOC_WW_Pin1_4 | 199 | 204 | PF00397 | 0.408 |
DOC_WW_Pin1_4 | 281 | 286 | PF00397 | 0.346 |
DOC_WW_Pin1_4 | 287 | 292 | PF00397 | 0.350 |
DOC_WW_Pin1_4 | 457 | 462 | PF00397 | 0.700 |
LIG_14-3-3_CanoR_1 | 172 | 177 | PF00244 | 0.424 |
LIG_14-3-3_CanoR_1 | 308 | 317 | PF00244 | 0.355 |
LIG_APCC_ABBA_1 | 227 | 232 | PF00400 | 0.447 |
LIG_BRCT_BRCA1_1 | 140 | 144 | PF00533 | 0.335 |
LIG_BRCT_BRCA1_1 | 34 | 38 | PF00533 | 0.507 |
LIG_Clathr_ClatBox_1 | 158 | 162 | PF01394 | 0.378 |
LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.672 |
LIG_FHA_1 | 195 | 201 | PF00498 | 0.355 |
LIG_FHA_1 | 269 | 275 | PF00498 | 0.434 |
LIG_FHA_1 | 383 | 389 | PF00498 | 0.420 |
LIG_FHA_1 | 406 | 412 | PF00498 | 0.481 |
LIG_FHA_1 | 89 | 95 | PF00498 | 0.473 |
LIG_FHA_2 | 453 | 459 | PF00498 | 0.593 |
LIG_HP1_1 | 120 | 124 | PF01393 | 0.378 |
LIG_LIR_Apic_2 | 141 | 147 | PF02991 | 0.408 |
LIG_LIR_Apic_2 | 175 | 179 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 180 | 189 | PF02991 | 0.378 |
LIG_LIR_Gen_1 | 284 | 294 | PF02991 | 0.395 |
LIG_LIR_Gen_1 | 35 | 45 | PF02991 | 0.430 |
LIG_LIR_Gen_1 | 408 | 417 | PF02991 | 0.501 |
LIG_LIR_Nem_3 | 180 | 184 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 205 | 211 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 254 | 260 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 284 | 289 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 35 | 41 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 358 | 363 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 387 | 393 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 408 | 413 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 434 | 439 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 458 | 462 | PF02991 | 0.554 |
LIG_NRP_CendR_1 | 502 | 505 | PF00754 | 0.713 |
LIG_Pex14_2 | 167 | 171 | PF04695 | 0.355 |
LIG_Pex14_2 | 448 | 452 | PF04695 | 0.582 |
LIG_PTB_Apo_2 | 322 | 329 | PF02174 | 0.335 |
LIG_PTB_Phospho_1 | 322 | 328 | PF10480 | 0.335 |
LIG_Rb_LxCxE_1 | 215 | 232 | PF01857 | 0.447 |
LIG_SH2_CRK | 459 | 463 | PF00017 | 0.563 |
LIG_SH2_PTP2 | 410 | 413 | PF00017 | 0.568 |
LIG_SH2_SRC | 176 | 179 | PF00017 | 0.447 |
LIG_SH2_STAP1 | 355 | 359 | PF00017 | 0.411 |
LIG_SH2_STAT3 | 439 | 442 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 176 | 179 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 217 | 220 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 230 | 233 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 328 | 331 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 390 | 393 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 410 | 413 | PF00017 | 0.271 |
LIG_SH2_STAT5 | 424 | 427 | PF00017 | 0.350 |
LIG_SH2_STAT5 | 439 | 442 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 459 | 462 | PF00017 | 0.388 |
LIG_SH3_3 | 114 | 120 | PF00018 | 0.496 |
LIG_SH3_3 | 181 | 187 | PF00018 | 0.447 |
LIG_SH3_3 | 410 | 416 | PF00018 | 0.530 |
LIG_SH3_3 | 48 | 54 | PF00018 | 0.553 |
LIG_Sin3_3 | 38 | 45 | PF02671 | 0.538 |
LIG_SUMO_SIM_par_1 | 156 | 162 | PF11976 | 0.378 |
LIG_TRAF2_1 | 31 | 34 | PF00917 | 0.488 |
LIG_TRAF2_1 | 99 | 102 | PF00917 | 0.432 |
LIG_TYR_ITIM | 388 | 393 | PF00017 | 0.445 |
LIG_TYR_ITSM | 406 | 413 | PF00017 | 0.513 |
LIG_UBA3_1 | 1 | 5 | PF00899 | 0.661 |
MOD_CDK_SPK_2 | 143 | 148 | PF00069 | 0.447 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.339 |
MOD_CK1_1 | 405 | 411 | PF00069 | 0.577 |
MOD_CK1_1 | 88 | 94 | PF00069 | 0.533 |
MOD_CK2_1 | 337 | 343 | PF00069 | 0.524 |
MOD_CK2_1 | 452 | 458 | PF00069 | 0.623 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.335 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.403 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.368 |
MOD_GlcNHglycan | 404 | 407 | PF01048 | 0.564 |
MOD_GlcNHglycan | 482 | 485 | PF01048 | 0.692 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.335 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.408 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.531 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.481 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.511 |
MOD_GSK3_1 | 476 | 483 | PF00069 | 0.678 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.550 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.335 |
MOD_NEK2_1 | 26 | 31 | PF00069 | 0.539 |
MOD_NEK2_1 | 323 | 328 | PF00069 | 0.336 |
MOD_NEK2_1 | 452 | 457 | PF00069 | 0.643 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.452 |
MOD_NEK2_2 | 293 | 298 | PF00069 | 0.404 |
MOD_PIKK_1 | 308 | 314 | PF00454 | 0.355 |
MOD_PIKK_1 | 333 | 339 | PF00454 | 0.459 |
MOD_PIKK_1 | 80 | 86 | PF00454 | 0.521 |
MOD_PKA_2 | 88 | 94 | PF00069 | 0.483 |
MOD_Plk_1 | 194 | 200 | PF00069 | 0.349 |
MOD_Plk_2-3 | 389 | 395 | PF00069 | 0.480 |
MOD_Plk_4 | 153 | 159 | PF00069 | 0.334 |
MOD_Plk_4 | 293 | 299 | PF00069 | 0.404 |
MOD_Plk_4 | 323 | 329 | PF00069 | 0.331 |
MOD_ProDKin_1 | 143 | 149 | PF00069 | 0.384 |
MOD_ProDKin_1 | 151 | 157 | PF00069 | 0.319 |
MOD_ProDKin_1 | 199 | 205 | PF00069 | 0.408 |
MOD_ProDKin_1 | 281 | 287 | PF00069 | 0.346 |
MOD_ProDKin_1 | 457 | 463 | PF00069 | 0.695 |
MOD_SUMO_rev_2 | 445 | 452 | PF00179 | 0.542 |
TRG_DiLeu_BaEn_4 | 101 | 107 | PF01217 | 0.460 |
TRG_DiLeu_BaLyEn_6 | 19 | 24 | PF01217 | 0.579 |
TRG_ENDOCYTIC_2 | 230 | 233 | PF00928 | 0.347 |
TRG_ENDOCYTIC_2 | 283 | 286 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 360 | 363 | PF00928 | 0.497 |
TRG_ENDOCYTIC_2 | 390 | 393 | PF00928 | 0.428 |
TRG_ENDOCYTIC_2 | 398 | 401 | PF00928 | 0.419 |
TRG_ENDOCYTIC_2 | 410 | 413 | PF00928 | 0.271 |
TRG_ENDOCYTIC_2 | 424 | 427 | PF00928 | 0.310 |
TRG_ENDOCYTIC_2 | 459 | 462 | PF00928 | 0.550 |
TRG_ER_diArg_1 | 233 | 235 | PF00400 | 0.408 |
TRG_ER_diArg_1 | 366 | 368 | PF00400 | 0.516 |
TRG_ER_diArg_1 | 398 | 400 | PF00400 | 0.426 |
TRG_ER_diArg_1 | 86 | 89 | PF00400 | 0.430 |
TRG_NLS_MonoExtC_3 | 167 | 172 | PF00514 | 0.402 |
TRG_NLS_MonoExtN_4 | 168 | 173 | PF00514 | 0.402 |
TRG_Pf-PMV_PEXEL_1 | 308 | 312 | PF00026 | 0.335 |
TRG_Pf-PMV_PEXEL_1 | 415 | 419 | PF00026 | 0.438 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HU64 | Leptomonas seymouri | 84% | 100% |
A0A0S4J6G2 | Bodo saltans | 50% | 100% |
A0A1X0NNJ1 | Trypanosomatidae | 62% | 100% |
A0A3S7WT30 | Leishmania donovani | 100% | 100% |
A4H7Q6 | Leishmania braziliensis | 92% | 100% |
C9ZSX6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 61% | 100% |
E9APU8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 100% |
Q4QFN2 | Leishmania major | 98% | 100% |
V5BNF0 | Trypanosoma cruzi | 60% | 100% |