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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A4HJY4
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0005488 | binding | 1 | 4 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
GO:0043167 | ion binding | 2 | 3 |
GO:0043169 | cation binding | 3 | 3 |
GO:0046872 | metal ion binding | 4 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 121 | 123 | PF00675 | 0.443 |
CLV_NRD_NRD_1 | 59 | 61 | PF00675 | 0.485 |
CLV_NRD_NRD_1 | 68 | 70 | PF00675 | 0.567 |
CLV_PCSK_KEX2_1 | 121 | 123 | PF00082 | 0.430 |
CLV_PCSK_KEX2_1 | 68 | 70 | PF00082 | 0.537 |
CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 21 | 25 | PF00082 | 0.471 |
CLV_PCSK_SKI1_1 | 68 | 72 | PF00082 | 0.525 |
CLV_PCSK_SKI1_1 | 73 | 77 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.445 |
CLV_PCSK_SKI1_1 | 93 | 97 | PF00082 | 0.266 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.525 |
DEG_SPOP_SBC_1 | 320 | 324 | PF00917 | 0.546 |
DOC_CYCLIN_RxL_1 | 119 | 129 | PF00134 | 0.443 |
DOC_CYCLIN_RxL_1 | 73 | 82 | PF00134 | 0.291 |
DOC_MAPK_gen_1 | 18 | 28 | PF00069 | 0.459 |
DOC_MAPK_MEF2A_6 | 18 | 26 | PF00069 | 0.505 |
DOC_USP7_MATH_1 | 189 | 193 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 261 | 265 | PF00917 | 0.670 |
DOC_WW_Pin1_4 | 205 | 210 | PF00397 | 0.552 |
DOC_WW_Pin1_4 | 77 | 82 | PF00397 | 0.369 |
LIG_14-3-3_CanoR_1 | 103 | 109 | PF00244 | 0.595 |
LIG_14-3-3_CanoR_1 | 194 | 200 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 226 | 235 | PF00244 | 0.572 |
LIG_14-3-3_CanoR_1 | 281 | 285 | PF00244 | 0.642 |
LIG_14-3-3_CanoR_1 | 321 | 327 | PF00244 | 0.552 |
LIG_BRCT_BRCA1_1 | 149 | 153 | PF00533 | 0.309 |
LIG_FHA_1 | 109 | 115 | PF00498 | 0.402 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.607 |
LIG_FHA_2 | 127 | 133 | PF00498 | 0.501 |
LIG_FHA_2 | 284 | 290 | PF00498 | 0.531 |
LIG_LIR_Gen_1 | 211 | 221 | PF02991 | 0.643 |
LIG_LIR_Gen_1 | 234 | 243 | PF02991 | 0.634 |
LIG_LIR_Nem_3 | 206 | 210 | PF02991 | 0.600 |
LIG_LIR_Nem_3 | 211 | 217 | PF02991 | 0.648 |
LIG_LIR_Nem_3 | 234 | 238 | PF02991 | 0.592 |
LIG_NRBOX | 82 | 88 | PF00104 | 0.414 |
LIG_Pex14_2 | 28 | 32 | PF04695 | 0.490 |
LIG_REV1ctd_RIR_1 | 68 | 77 | PF16727 | 0.447 |
LIG_SH2_CRK | 214 | 218 | PF00017 | 0.672 |
LIG_SH2_GRB2like | 63 | 66 | PF00017 | 0.657 |
LIG_SH2_NCK_1 | 116 | 120 | PF00017 | 0.388 |
LIG_SH2_PTP2 | 63 | 66 | PF00017 | 0.404 |
LIG_SH2_SRC | 116 | 119 | PF00017 | 0.307 |
LIG_SH2_SRC | 63 | 66 | PF00017 | 0.404 |
LIG_SH2_STAP1 | 116 | 120 | PF00017 | 0.427 |
LIG_SH2_STAP1 | 214 | 218 | PF00017 | 0.515 |
LIG_SH2_STAT5 | 63 | 66 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 99 | 102 | PF00017 | 0.404 |
LIG_TRAF2_1 | 323 | 326 | PF00917 | 0.552 |
LIG_UBA3_1 | 55 | 61 | PF00899 | 0.348 |
LIG_UBA3_1 | 86 | 93 | PF00899 | 0.458 |
LIG_WRC_WIRS_1 | 204 | 209 | PF05994 | 0.486 |
LIG_WRC_WIRS_1 | 29 | 34 | PF05994 | 0.509 |
MOD_CDK_SPxxK_3 | 77 | 84 | PF00069 | 0.367 |
MOD_CK1_1 | 126 | 132 | PF00069 | 0.486 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.391 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.476 |
MOD_CK1_1 | 264 | 270 | PF00069 | 0.738 |
MOD_CK1_1 | 283 | 289 | PF00069 | 0.604 |
MOD_CK1_1 | 336 | 342 | PF00069 | 0.713 |
MOD_CK2_1 | 126 | 132 | PF00069 | 0.592 |
MOD_CK2_1 | 283 | 289 | PF00069 | 0.531 |
MOD_CK2_1 | 319 | 325 | PF00069 | 0.590 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.397 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.725 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.611 |
MOD_GlcNHglycan | 325 | 330 | PF01048 | 0.624 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.570 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.384 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.653 |
MOD_GSK3_1 | 289 | 296 | PF00069 | 0.675 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.609 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.468 |
MOD_N-GLC_1 | 264 | 269 | PF02516 | 0.635 |
MOD_N-GLC_1 | 301 | 306 | PF02516 | 0.546 |
MOD_N-GLC_1 | 307 | 312 | PF02516 | 0.595 |
MOD_N-GLC_1 | 314 | 319 | PF02516 | 0.664 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.404 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.500 |
MOD_NEK2_1 | 319 | 324 | PF00069 | 0.588 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.464 |
MOD_PIKK_1 | 182 | 188 | PF00454 | 0.487 |
MOD_PIKK_1 | 283 | 289 | PF00454 | 0.670 |
MOD_PKA_2 | 102 | 108 | PF00069 | 0.468 |
MOD_PKA_2 | 280 | 286 | PF00069 | 0.537 |
MOD_PKA_2 | 320 | 326 | PF00069 | 0.550 |
MOD_PKB_1 | 224 | 232 | PF00069 | 0.530 |
MOD_Plk_1 | 264 | 270 | PF00069 | 0.674 |
MOD_Plk_4 | 280 | 286 | PF00069 | 0.597 |
MOD_ProDKin_1 | 205 | 211 | PF00069 | 0.553 |
MOD_ProDKin_1 | 77 | 83 | PF00069 | 0.364 |
MOD_SUMO_rev_2 | 310 | 316 | PF00179 | 0.601 |
TRG_DiLeu_BaEn_1 | 82 | 87 | PF01217 | 0.448 |
TRG_DiLeu_LyEn_5 | 19 | 24 | PF01217 | 0.473 |
TRG_ENDOCYTIC_2 | 214 | 217 | PF00928 | 0.673 |
TRG_ER_diArg_1 | 120 | 122 | PF00400 | 0.424 |
TRG_ER_diArg_1 | 223 | 226 | PF00400 | 0.618 |
TRG_ER_diArg_1 | 68 | 70 | PF00400 | 0.528 |
TRG_Pf-PMV_PEXEL_1 | 176 | 180 | PF00026 | 0.402 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I963 | Leptomonas seymouri | 58% | 90% |
A0A3S7X526 | Leishmania donovani | 70% | 100% |
A4I7G7 | Leishmania infantum | 70% | 100% |
E9B2C4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 68% | 100% |
Q4Q5T2 | Leishmania major | 70% | 100% |