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. | yes | yes: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: A0A3S7X500
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 9 |
GO:0043167 | ion binding | 2 | 9 |
GO:0043169 | cation binding | 3 | 9 |
GO:0046872 | metal ion binding | 4 | 9 |
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 112 | 116 | PF00656 | 0.392 |
CLV_C14_Caspase3-7 | 345 | 349 | PF00656 | 0.527 |
CLV_NRD_NRD_1 | 117 | 119 | PF00675 | 0.505 |
CLV_NRD_NRD_1 | 151 | 153 | PF00675 | 0.372 |
CLV_NRD_NRD_1 | 189 | 191 | PF00675 | 0.542 |
CLV_PCSK_KEX2_1 | 110 | 112 | PF00082 | 0.432 |
CLV_PCSK_KEX2_1 | 150 | 152 | PF00082 | 0.470 |
CLV_PCSK_PC1ET2_1 | 110 | 112 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 111 | 115 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 131 | 135 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 152 | 156 | PF00082 | 0.421 |
CLV_PCSK_SKI1_1 | 235 | 239 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 241 | 245 | PF00082 | 0.443 |
CLV_PCSK_SKI1_1 | 352 | 356 | PF00082 | 0.546 |
DEG_APCC_DBOX_1 | 110 | 118 | PF00400 | 0.392 |
DEG_APCC_DBOX_1 | 151 | 159 | PF00400 | 0.422 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.617 |
DOC_MAPK_gen_1 | 99 | 109 | PF00069 | 0.480 |
DOC_MAPK_HePTP_8 | 73 | 85 | PF00069 | 0.508 |
DOC_MAPK_MEF2A_6 | 76 | 85 | PF00069 | 0.491 |
DOC_PP2B_LxvP_1 | 284 | 287 | PF13499 | 0.575 |
DOC_PP4_FxxP_1 | 282 | 285 | PF00568 | 0.716 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 39 | 43 | PF00917 | 0.497 |
DOC_USP7_UBL2_3 | 191 | 195 | PF12436 | 0.500 |
DOC_USP7_UBL2_3 | 235 | 239 | PF12436 | 0.443 |
DOC_USP7_UBL2_3 | 91 | 95 | PF12436 | 0.518 |
DOC_WW_Pin1_4 | 265 | 270 | PF00397 | 0.669 |
DOC_WW_Pin1_4 | 296 | 301 | PF00397 | 0.540 |
DOC_WW_Pin1_4 | 317 | 322 | PF00397 | 0.749 |
LIG_14-3-3_CanoR_1 | 222 | 227 | PF00244 | 0.330 |
LIG_14-3-3_CanoR_1 | 352 | 359 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 76 | 82 | PF00244 | 0.479 |
LIG_BRCT_BRCA1_1 | 55 | 59 | PF00533 | 0.481 |
LIG_CtBP_PxDLS_1 | 329 | 333 | PF00389 | 0.529 |
LIG_eIF4E_1 | 22 | 28 | PF01652 | 0.491 |
LIG_EVH1_1 | 282 | 286 | PF00568 | 0.555 |
LIG_EVH1_2 | 303 | 307 | PF00568 | 0.547 |
LIG_FHA_1 | 160 | 166 | PF00498 | 0.392 |
LIG_FHA_1 | 22 | 28 | PF00498 | 0.459 |
LIG_FHA_1 | 266 | 272 | PF00498 | 0.620 |
LIG_FHA_1 | 56 | 62 | PF00498 | 0.512 |
LIG_FHA_2 | 170 | 176 | PF00498 | 0.409 |
LIG_FHA_2 | 31 | 37 | PF00498 | 0.403 |
LIG_LIR_Gen_1 | 138 | 149 | PF02991 | 0.404 |
LIG_LIR_Gen_1 | 357 | 366 | PF02991 | 0.621 |
LIG_LIR_Nem_3 | 138 | 144 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 348 | 354 | PF02991 | 0.557 |
LIG_LIR_Nem_3 | 357 | 362 | PF02991 | 0.581 |
LIG_Pex14_2 | 85 | 89 | PF04695 | 0.436 |
LIG_SH2_CRK | 121 | 125 | PF00017 | 0.502 |
LIG_SH2_CRK | 93 | 97 | PF00017 | 0.512 |
LIG_SH2_GRB2like | 121 | 124 | PF00017 | 0.502 |
LIG_SH2_NCK_1 | 121 | 125 | PF00017 | 0.491 |
LIG_SH2_STAP1 | 174 | 178 | PF00017 | 0.392 |
LIG_SH2_STAP1 | 23 | 27 | PF00017 | 0.456 |
LIG_SH2_STAT3 | 174 | 177 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 121 | 124 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 128 | 131 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.373 |
LIG_SH2_STAT5 | 23 | 26 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 305 | 308 | PF00017 | 0.626 |
LIG_SH3_3 | 268 | 274 | PF00018 | 0.626 |
LIG_SH3_3 | 280 | 286 | PF00018 | 0.643 |
LIG_SH3_3 | 294 | 300 | PF00018 | 0.549 |
LIG_SUMO_SIM_anti_2 | 33 | 39 | PF11976 | 0.434 |
LIG_SxIP_EBH_1 | 8 | 17 | PF03271 | 0.473 |
LIG_TRFH_1 | 282 | 286 | PF08558 | 0.494 |
LIG_WRC_WIRS_1 | 359 | 364 | PF05994 | 0.541 |
LIG_WRC_WIRS_1 | 86 | 91 | PF05994 | 0.468 |
LIG_WW_1 | 302 | 305 | PF00397 | 0.486 |
MOD_CDK_SPK_2 | 265 | 270 | PF00069 | 0.631 |
MOD_CDK_SPK_2 | 296 | 301 | PF00069 | 0.479 |
MOD_CK1_1 | 259 | 265 | PF00069 | 0.567 |
MOD_CK1_1 | 314 | 320 | PF00069 | 0.596 |
MOD_CK2_1 | 169 | 175 | PF00069 | 0.465 |
MOD_CK2_1 | 181 | 187 | PF00069 | 0.579 |
MOD_CK2_1 | 30 | 36 | PF00069 | 0.414 |
MOD_CK2_1 | 354 | 360 | PF00069 | 0.449 |
MOD_Cter_Amidation | 250 | 253 | PF01082 | 0.449 |
MOD_GlcNHglycan | 274 | 277 | PF01048 | 0.578 |
MOD_GlcNHglycan | 315 | 319 | PF01048 | 0.660 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.673 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.435 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.521 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.446 |
MOD_GSK3_1 | 317 | 324 | PF00069 | 0.679 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.536 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.508 |
MOD_N-GLC_1 | 135 | 140 | PF02516 | 0.401 |
MOD_N-GLC_1 | 77 | 82 | PF02516 | 0.530 |
MOD_N-GLC_2 | 209 | 211 | PF02516 | 0.376 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.445 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.415 |
MOD_NEK2_1 | 214 | 219 | PF00069 | 0.375 |
MOD_NEK2_1 | 295 | 300 | PF00069 | 0.579 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.724 |
MOD_NEK2_1 | 330 | 335 | PF00069 | 0.486 |
MOD_NEK2_1 | 6 | 11 | PF00069 | 0.646 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.475 |
MOD_OFUCOSY | 220 | 226 | PF10250 | 0.395 |
MOD_PIKK_1 | 260 | 266 | PF00454 | 0.605 |
MOD_PIKK_1 | 354 | 360 | PF00454 | 0.591 |
MOD_PIKK_1 | 44 | 50 | PF00454 | 0.488 |
MOD_PKA_1 | 252 | 258 | PF00069 | 0.540 |
MOD_PKA_2 | 189 | 195 | PF00069 | 0.536 |
MOD_Plk_1 | 330 | 336 | PF00069 | 0.731 |
MOD_Plk_1 | 77 | 83 | PF00069 | 0.560 |
MOD_Plk_2-3 | 159 | 165 | PF00069 | 0.409 |
MOD_Plk_2-3 | 30 | 36 | PF00069 | 0.366 |
MOD_Plk_4 | 143 | 149 | PF00069 | 0.394 |
MOD_Plk_4 | 252 | 258 | PF00069 | 0.540 |
MOD_Plk_4 | 30 | 36 | PF00069 | 0.420 |
MOD_ProDKin_1 | 265 | 271 | PF00069 | 0.670 |
MOD_ProDKin_1 | 296 | 302 | PF00069 | 0.537 |
MOD_ProDKin_1 | 317 | 323 | PF00069 | 0.749 |
MOD_SUMO_for_1 | 109 | 112 | PF00179 | 0.407 |
TRG_DiLeu_BaLyEn_6 | 349 | 354 | PF01217 | 0.531 |
TRG_ENDOCYTIC_2 | 157 | 160 | PF00928 | 0.393 |
TRG_ENDOCYTIC_2 | 93 | 96 | PF00928 | 0.510 |
TRG_ER_diArg_1 | 150 | 152 | PF00400 | 0.473 |
TRG_NLS_MonoExtN_4 | 188 | 194 | PF00514 | 0.481 |
TRG_Pf-PMV_PEXEL_1 | 25 | 30 | PF00026 | 0.501 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2H1 | Leptomonas seymouri | 60% | 100% |
A0A0S4JCY0 | Bodo saltans | 35% | 94% |
A0A3S7X526 | Leishmania donovani | 36% | 100% |
A4HJY2 | Leishmania braziliensis | 74% | 100% |
A4I7G6 | Leishmania infantum | 99% | 100% |
E9B2C3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
Q4Q5T3 | Leishmania major | 93% | 100% |