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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A4H4M7
Term | Name | Level | Count |
---|---|---|---|
GO:0009605 | response to external stimulus | 2 | 7 |
GO:0009991 | response to extracellular stimulus | 3 | 7 |
GO:0015976 | carbon utilization | 5 | 7 |
GO:0031667 | response to nutrient levels | 4 | 7 |
GO:0050896 | response to stimulus | 1 | 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0004089 | carbonate dehydratase activity | 5 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0008270 | zinc ion binding | 6 | 7 |
GO:0016829 | lyase activity | 2 | 7 |
GO:0016835 | carbon-oxygen lyase activity | 3 | 7 |
GO:0016836 | hydro-lyase activity | 4 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043169 | cation binding | 3 | 7 |
GO:0046872 | metal ion binding | 4 | 7 |
GO:0046914 | transition metal ion binding | 5 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 17 | 19 | PF00675 | 0.502 |
CLV_NRD_NRD_1 | 282 | 284 | PF00675 | 0.361 |
CLV_NRD_NRD_1 | 366 | 368 | PF00675 | 0.369 |
CLV_PCSK_KEX2_1 | 17 | 19 | PF00082 | 0.502 |
CLV_PCSK_KEX2_1 | 278 | 280 | PF00082 | 0.280 |
CLV_PCSK_KEX2_1 | 282 | 284 | PF00082 | 0.280 |
CLV_PCSK_KEX2_1 | 366 | 368 | PF00082 | 0.369 |
CLV_PCSK_PC1ET2_1 | 278 | 280 | PF00082 | 0.280 |
CLV_PCSK_SKI1_1 | 282 | 286 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 359 | 363 | PF00082 | 0.386 |
CLV_Separin_Metazoa | 110 | 114 | PF03568 | 0.479 |
CLV_Separin_Metazoa | 167 | 171 | PF03568 | 0.295 |
DEG_APCC_DBOX_1 | 281 | 289 | PF00400 | 0.332 |
DEG_APCC_DBOX_1 | 290 | 298 | PF00400 | 0.236 |
DOC_ANK_TNKS_1 | 60 | 67 | PF00023 | 0.435 |
DOC_CKS1_1 | 106 | 111 | PF01111 | 0.464 |
DOC_CYCLIN_RxL_1 | 356 | 363 | PF00134 | 0.355 |
DOC_MAPK_gen_1 | 337 | 346 | PF00069 | 0.198 |
DOC_MAPK_JIP1_4 | 184 | 190 | PF00069 | 0.361 |
DOC_PP2B_LxvP_1 | 98 | 101 | PF13499 | 0.551 |
DOC_PP4_FxxP_1 | 4 | 7 | PF00568 | 0.530 |
DOC_USP7_MATH_1 | 101 | 105 | PF00917 | 0.515 |
DOC_USP7_MATH_1 | 149 | 153 | PF00917 | 0.448 |
DOC_USP7_MATH_1 | 9 | 13 | PF00917 | 0.686 |
DOC_USP7_UBL2_3 | 372 | 376 | PF12436 | 0.288 |
DOC_WW_Pin1_4 | 105 | 110 | PF00397 | 0.547 |
DOC_WW_Pin1_4 | 117 | 122 | PF00397 | 0.616 |
DOC_WW_Pin1_4 | 65 | 70 | PF00397 | 0.486 |
DOC_WW_Pin1_4 | 78 | 83 | PF00397 | 0.426 |
LIG_14-3-3_CanoR_1 | 138 | 144 | PF00244 | 0.515 |
LIG_14-3-3_CanoR_1 | 359 | 365 | PF00244 | 0.370 |
LIG_14-3-3_CanoR_1 | 366 | 371 | PF00244 | 0.398 |
LIG_14-3-3_CanoR_1 | 45 | 49 | PF00244 | 0.426 |
LIG_eIF4E_1 | 106 | 112 | PF01652 | 0.464 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.510 |
LIG_FHA_1 | 253 | 259 | PF00498 | 0.473 |
LIG_FHA_1 | 310 | 316 | PF00498 | 0.280 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.395 |
LIG_FHA_1 | 95 | 101 | PF00498 | 0.623 |
LIG_FHA_2 | 105 | 111 | PF00498 | 0.603 |
LIG_LIR_Apic_2 | 104 | 109 | PF02991 | 0.461 |
LIG_LIR_Gen_1 | 174 | 180 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 174 | 179 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 379 | 385 | PF02991 | 0.535 |
LIG_Pex14_2 | 4 | 8 | PF04695 | 0.436 |
LIG_PTB_Apo_2 | 169 | 176 | PF02174 | 0.383 |
LIG_PTB_Phospho_1 | 169 | 175 | PF10480 | 0.383 |
LIG_SH2_NCK_1 | 106 | 110 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 106 | 109 | PF00017 | 0.606 |
LIG_SH2_STAT5 | 175 | 178 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 187 | 190 | PF00017 | 0.317 |
LIG_SH3_3 | 90 | 96 | PF00018 | 0.543 |
LIG_SH3_5 | 156 | 160 | PF00018 | 0.298 |
LIG_Sin3_3 | 227 | 234 | PF02671 | 0.280 |
LIG_WW_3 | 147 | 151 | PF00397 | 0.456 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.413 |
MOD_CK1_1 | 120 | 126 | PF00069 | 0.562 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.711 |
MOD_CK1_1 | 68 | 74 | PF00069 | 0.528 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.593 |
MOD_CK2_1 | 104 | 110 | PF00069 | 0.600 |
MOD_CK2_1 | 365 | 371 | PF00069 | 0.372 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.658 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.433 |
MOD_GlcNHglycan | 245 | 248 | PF01048 | 0.313 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.280 |
MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.618 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.553 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.586 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.565 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.505 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.477 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.536 |
MOD_NEK2_1 | 271 | 276 | PF00069 | 0.280 |
MOD_NEK2_1 | 29 | 34 | PF00069 | 0.476 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.468 |
MOD_NEK2_2 | 101 | 106 | PF00069 | 0.469 |
MOD_PIKK_1 | 122 | 128 | PF00454 | 0.440 |
MOD_PIKK_1 | 317 | 323 | PF00454 | 0.231 |
MOD_PK_1 | 366 | 372 | PF00069 | 0.298 |
MOD_PKA_1 | 366 | 372 | PF00069 | 0.298 |
MOD_PKA_2 | 149 | 155 | PF00069 | 0.440 |
MOD_PKA_2 | 16 | 22 | PF00069 | 0.484 |
MOD_PKA_2 | 333 | 339 | PF00069 | 0.290 |
MOD_PKA_2 | 365 | 371 | PF00069 | 0.387 |
MOD_PKA_2 | 39 | 45 | PF00069 | 0.507 |
MOD_PKA_2 | 94 | 100 | PF00069 | 0.613 |
MOD_PKB_1 | 113 | 121 | PF00069 | 0.493 |
MOD_Plk_1 | 113 | 119 | PF00069 | 0.652 |
MOD_Plk_4 | 101 | 107 | PF00069 | 0.615 |
MOD_Plk_4 | 130 | 136 | PF00069 | 0.536 |
MOD_Plk_4 | 25 | 31 | PF00069 | 0.481 |
MOD_ProDKin_1 | 105 | 111 | PF00069 | 0.547 |
MOD_ProDKin_1 | 117 | 123 | PF00069 | 0.609 |
MOD_ProDKin_1 | 65 | 71 | PF00069 | 0.487 |
MOD_ProDKin_1 | 78 | 84 | PF00069 | 0.423 |
MOD_SUMO_for_1 | 127 | 130 | PF00179 | 0.435 |
MOD_SUMO_for_1 | 238 | 241 | PF00179 | 0.270 |
TRG_DiLeu_BaEn_1 | 130 | 135 | PF01217 | 0.448 |
TRG_DiLeu_BaLyEn_6 | 153 | 158 | PF01217 | 0.408 |
TRG_DiLeu_BaLyEn_6 | 357 | 362 | PF01217 | 0.350 |
TRG_ENDOCYTIC_2 | 187 | 190 | PF00928 | 0.317 |
TRG_ENDOCYTIC_2 | 385 | 388 | PF00928 | 0.397 |
TRG_ER_diArg_1 | 16 | 18 | PF00400 | 0.488 |
TRG_ER_diArg_1 | 281 | 283 | PF00400 | 0.393 |
TRG_ER_diArg_1 | 337 | 340 | PF00400 | 0.198 |
TRG_ER_diArg_1 | 58 | 61 | PF00400 | 0.644 |
TRG_Pf-PMV_PEXEL_1 | 283 | 287 | PF00026 | 0.440 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HX68 | Leptomonas seymouri | 69% | 99% |
A0A3S5H5R2 | Leishmania donovani | 88% | 100% |
A4HSV2 | Leishmania infantum | 88% | 100% |
E9AKU0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
O94255 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 34% | 100% |
Q4QJ17 | Leishmania major | 87% | 100% |