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:0005730 | nucleolus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HKS2
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003723 | RNA binding | 4 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 56 | 60 | PF00656 | 0.602 |
CLV_NRD_NRD_1 | 15 | 17 | PF00675 | 0.466 |
CLV_NRD_NRD_1 | 24 | 26 | PF00675 | 0.445 |
CLV_NRD_NRD_1 | 248 | 250 | PF00675 | 0.621 |
CLV_NRD_NRD_1 | 292 | 294 | PF00675 | 0.341 |
CLV_NRD_NRD_1 | 324 | 326 | PF00675 | 0.503 |
CLV_NRD_NRD_1 | 398 | 400 | PF00675 | 0.381 |
CLV_NRD_NRD_1 | 60 | 62 | PF00675 | 0.601 |
CLV_NRD_NRD_1 | 7 | 9 | PF00675 | 0.534 |
CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.215 |
CLV_PCSK_KEX2_1 | 200 | 202 | PF00082 | 0.451 |
CLV_PCSK_KEX2_1 | 247 | 249 | PF00082 | 0.482 |
CLV_PCSK_KEX2_1 | 324 | 326 | PF00082 | 0.503 |
CLV_PCSK_KEX2_1 | 398 | 400 | PF00082 | 0.383 |
CLV_PCSK_KEX2_1 | 443 | 445 | PF00082 | 0.419 |
CLV_PCSK_KEX2_1 | 57 | 59 | PF00082 | 0.589 |
CLV_PCSK_KEX2_1 | 62 | 64 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 7 | 9 | PF00082 | 0.533 |
CLV_PCSK_KEX2_1 | 80 | 82 | PF00082 | 0.471 |
CLV_PCSK_PC1ET2_1 | 138 | 140 | PF00082 | 0.289 |
CLV_PCSK_PC1ET2_1 | 200 | 202 | PF00082 | 0.451 |
CLV_PCSK_PC1ET2_1 | 247 | 249 | PF00082 | 0.482 |
CLV_PCSK_PC1ET2_1 | 443 | 445 | PF00082 | 0.407 |
CLV_PCSK_PC1ET2_1 | 57 | 59 | PF00082 | 0.589 |
CLV_PCSK_PC1ET2_1 | 62 | 64 | PF00082 | 0.587 |
CLV_PCSK_PC1ET2_1 | 7 | 9 | PF00082 | 0.550 |
CLV_PCSK_PC1ET2_1 | 80 | 82 | PF00082 | 0.471 |
CLV_PCSK_PC7_1 | 58 | 64 | PF00082 | 0.605 |
CLV_PCSK_SKI1_1 | 138 | 142 | PF00082 | 0.209 |
CLV_PCSK_SKI1_1 | 316 | 320 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 324 | 328 | PF00082 | 0.347 |
CLV_PCSK_SKI1_1 | 354 | 358 | PF00082 | 0.209 |
CLV_PCSK_SKI1_1 | 40 | 44 | PF00082 | 0.558 |
CLV_PCSK_SKI1_1 | 419 | 423 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 8 | 12 | PF00082 | 0.596 |
DEG_APCC_DBOX_1 | 39 | 47 | PF00400 | 0.393 |
DOC_CYCLIN_RxL_1 | 112 | 123 | PF00134 | 0.409 |
DOC_CYCLIN_yCln2_LP_2 | 436 | 442 | PF00134 | 0.421 |
DOC_MAPK_gen_1 | 221 | 230 | PF00069 | 0.514 |
DOC_MAPK_gen_1 | 398 | 404 | PF00069 | 0.333 |
DOC_MAPK_MEF2A_6 | 40 | 48 | PF00069 | 0.396 |
DOC_MAPK_RevD_3 | 44 | 58 | PF00069 | 0.441 |
DOC_PP2B_LxvP_1 | 267 | 270 | PF13499 | 0.373 |
DOC_PP2B_LxvP_1 | 436 | 439 | PF13499 | 0.419 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 363 | 367 | PF00917 | 0.420 |
DOC_USP7_MATH_1 | 442 | 446 | PF00917 | 0.474 |
DOC_USP7_UBL2_3 | 247 | 251 | PF12436 | 0.494 |
DOC_USP7_UBL2_3 | 3 | 7 | PF12436 | 0.631 |
DOC_USP7_UBL2_3 | 31 | 35 | PF12436 | 0.495 |
DOC_WW_Pin1_4 | 132 | 137 | PF00397 | 0.416 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.499 |
LIG_14-3-3_CanoR_1 | 146 | 152 | PF00244 | 0.445 |
LIG_14-3-3_CanoR_1 | 308 | 312 | PF00244 | 0.378 |
LIG_14-3-3_CanoR_1 | 316 | 323 | PF00244 | 0.382 |
LIG_14-3-3_CanoR_1 | 399 | 405 | PF00244 | 0.309 |
LIG_14-3-3_CterR_2 | 444 | 446 | PF00244 | 0.412 |
LIG_Actin_WH2_2 | 408 | 424 | PF00022 | 0.566 |
LIG_AP2alpha_2 | 215 | 217 | PF02296 | 0.356 |
LIG_BRCT_BRCA1_1 | 299 | 303 | PF00533 | 0.374 |
LIG_CaM_IQ_9 | 409 | 424 | PF13499 | 0.362 |
LIG_FHA_1 | 152 | 158 | PF00498 | 0.431 |
LIG_FHA_1 | 189 | 195 | PF00498 | 0.483 |
LIG_FHA_1 | 360 | 366 | PF00498 | 0.512 |
LIG_FHA_1 | 39 | 45 | PF00498 | 0.390 |
LIG_FHA_1 | 407 | 413 | PF00498 | 0.376 |
LIG_FHA_2 | 119 | 125 | PF00498 | 0.421 |
LIG_FHA_2 | 315 | 321 | PF00498 | 0.391 |
LIG_LIR_Gen_1 | 222 | 231 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 132 | 137 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 222 | 228 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 366 | 372 | PF02991 | 0.429 |
LIG_MLH1_MIPbox_1 | 299 | 303 | PF16413 | 0.503 |
LIG_Pex14_2 | 130 | 134 | PF04695 | 0.410 |
LIG_PTB_Apo_2 | 296 | 303 | PF02174 | 0.499 |
LIG_REV1ctd_RIR_1 | 215 | 225 | PF16727 | 0.255 |
LIG_REV1ctd_RIR_1 | 300 | 310 | PF16727 | 0.241 |
LIG_SH2_CRK | 350 | 354 | PF00017 | 0.420 |
LIG_SH2_STAT3 | 171 | 174 | PF00017 | 0.509 |
LIG_SH2_STAT3 | 261 | 264 | PF00017 | 0.373 |
LIG_SH2_STAT5 | 129 | 132 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 261 | 264 | PF00017 | 0.339 |
LIG_SH2_STAT5 | 282 | 285 | PF00017 | 0.399 |
LIG_SH2_STAT5 | 334 | 337 | PF00017 | 0.456 |
LIG_SH3_3 | 210 | 216 | PF00018 | 0.544 |
LIG_TRAF2_1 | 121 | 124 | PF00917 | 0.435 |
LIG_WRC_WIRS_1 | 401 | 406 | PF05994 | 0.306 |
MOD_CDC14_SPxK_1 | 135 | 138 | PF00782 | 0.256 |
MOD_CDK_SPxK_1 | 132 | 138 | PF00069 | 0.256 |
MOD_CDK_SPxxK_3 | 132 | 139 | PF00069 | 0.256 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.547 |
MOD_CK2_1 | 118 | 124 | PF00069 | 0.247 |
MOD_CK2_1 | 314 | 320 | PF00069 | 0.381 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.282 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.326 |
MOD_GlcNHglycan | 178 | 182 | PF01048 | 0.382 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.464 |
MOD_GlcNHglycan | 271 | 274 | PF01048 | 0.458 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.732 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.384 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.119 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.483 |
MOD_GSK3_1 | 229 | 236 | PF00069 | 0.455 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.261 |
MOD_N-GLC_2 | 408 | 410 | PF02516 | 0.251 |
MOD_NEK2_1 | 151 | 156 | PF00069 | 0.258 |
MOD_NEK2_1 | 220 | 225 | PF00069 | 0.432 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.403 |
MOD_NEK2_1 | 359 | 364 | PF00069 | 0.390 |
MOD_NEK2_1 | 400 | 405 | PF00069 | 0.319 |
MOD_NEK2_2 | 2 | 7 | PF00069 | 0.600 |
MOD_NEK2_2 | 380 | 385 | PF00069 | 0.340 |
MOD_PIKK_1 | 107 | 113 | PF00454 | 0.426 |
MOD_PIKK_1 | 233 | 239 | PF00454 | 0.461 |
MOD_PKA_1 | 247 | 253 | PF00069 | 0.503 |
MOD_PKA_1 | 57 | 63 | PF00069 | 0.635 |
MOD_PKA_2 | 145 | 151 | PF00069 | 0.308 |
MOD_PKA_2 | 220 | 226 | PF00069 | 0.346 |
MOD_PKA_2 | 247 | 253 | PF00069 | 0.385 |
MOD_PKA_2 | 307 | 313 | PF00069 | 0.387 |
MOD_PKA_2 | 57 | 63 | PF00069 | 0.484 |
MOD_PKB_1 | 61 | 69 | PF00069 | 0.722 |
MOD_Plk_1 | 177 | 183 | PF00069 | 0.507 |
MOD_Plk_1 | 73 | 79 | PF00069 | 0.700 |
MOD_Plk_2-3 | 89 | 95 | PF00069 | 0.545 |
MOD_Plk_4 | 125 | 131 | PF00069 | 0.390 |
MOD_Plk_4 | 207 | 213 | PF00069 | 0.598 |
MOD_Plk_4 | 389 | 395 | PF00069 | 0.365 |
MOD_ProDKin_1 | 132 | 138 | PF00069 | 0.256 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.492 |
MOD_SUMO_rev_2 | 180 | 189 | PF00179 | 0.589 |
TRG_DiLeu_BaEn_2 | 108 | 114 | PF01217 | 0.405 |
TRG_ENDOCYTIC_2 | 282 | 285 | PF00928 | 0.362 |
TRG_ENDOCYTIC_2 | 350 | 353 | PF00928 | 0.261 |
TRG_ENDOCYTIC_2 | 369 | 372 | PF00928 | 0.246 |
TRG_ER_diArg_1 | 143 | 146 | PF00400 | 0.272 |
TRG_ER_diArg_1 | 323 | 325 | PF00400 | 0.487 |
TRG_ER_diArg_1 | 398 | 400 | PF00400 | 0.327 |
TRG_ER_diArg_1 | 61 | 64 | PF00400 | 0.637 |
TRG_ER_diLys_1 | 441 | 446 | PF00400 | 0.570 |
TRG_NLS_Bipartite_1 | 7 | 21 | PF00514 | 0.486 |
TRG_NLS_MonoCore_2 | 15 | 20 | PF00514 | 0.477 |
TRG_NLS_MonoCore_2 | 244 | 249 | PF00514 | 0.484 |
TRG_NLS_MonoCore_2 | 61 | 66 | PF00514 | 0.496 |
TRG_NLS_MonoExtC_3 | 244 | 249 | PF00514 | 0.468 |
TRG_NLS_MonoExtC_3 | 60 | 65 | PF00514 | 0.583 |
TRG_NLS_MonoExtN_4 | 16 | 21 | PF00514 | 0.473 |
TRG_NLS_MonoExtN_4 | 245 | 251 | PF00514 | 0.476 |
TRG_NLS_MonoExtN_4 | 31 | 38 | PF00514 | 0.565 |
TRG_NLS_MonoExtN_4 | 58 | 65 | PF00514 | 0.614 |
TRG_Pf-PMV_PEXEL_1 | 324 | 329 | PF00026 | 0.449 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8M4 | Leptomonas seymouri | 85% | 100% |
A0A0S4IWT2 | Bodo saltans | 55% | 100% |
A0A1X0NSA9 | Trypanosomatidae | 63% | 100% |
A0A3Q8IG48 | Leishmania donovani | 89% | 100% |
A0A3R7N0S8 | Trypanosoma rangeli | 62% | 100% |
A4I8A2 | Leishmania infantum | 89% | 100% |
D0AAH4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 60% | 100% |
E9B360 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
O74400 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 26% | 66% |
Q4Q4Z4 | Leishmania major | 88% | 100% |
V5BDC2 | Trypanosoma cruzi | 63% | 92% |