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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: E9ADP3
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 2 |
GO:0003723 | RNA binding | 4 | 2 |
GO:0005488 | binding | 1 | 6 |
GO:0043167 | ion binding | 2 | 6 |
GO:0043169 | cation binding | 3 | 6 |
GO:0046872 | metal ion binding | 4 | 6 |
GO:0097159 | organic cyclic compound binding | 2 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 186 | 190 | PF00656 | 0.630 |
CLV_C14_Caspase3-7 | 275 | 279 | PF00656 | 0.639 |
CLV_C14_Caspase3-7 | 364 | 368 | PF00656 | 0.556 |
CLV_NRD_NRD_1 | 335 | 337 | PF00675 | 0.580 |
CLV_NRD_NRD_1 | 57 | 59 | PF00675 | 0.538 |
CLV_PCSK_FUR_1 | 333 | 337 | PF00082 | 0.446 |
CLV_PCSK_KEX2_1 | 333 | 335 | PF00082 | 0.597 |
CLV_PCSK_KEX2_1 | 57 | 59 | PF00082 | 0.538 |
CLV_PCSK_SKI1_1 | 15 | 19 | PF00082 | 0.636 |
CLV_PCSK_SKI1_1 | 219 | 223 | PF00082 | 0.551 |
CLV_PCSK_SKI1_1 | 232 | 236 | PF00082 | 0.450 |
CLV_PCSK_SKI1_1 | 300 | 304 | PF00082 | 0.691 |
DEG_APCC_DBOX_1 | 218 | 226 | PF00400 | 0.546 |
DEG_SPOP_SBC_1 | 137 | 141 | PF00917 | 0.651 |
DOC_CKS1_1 | 102 | 107 | PF01111 | 0.690 |
DOC_CYCLIN_RxL_1 | 297 | 305 | PF00134 | 0.561 |
DOC_CYCLIN_RxL_1 | 9 | 22 | PF00134 | 0.635 |
DOC_MAPK_gen_1 | 5 | 13 | PF00069 | 0.642 |
DOC_MAPK_gen_1 | 57 | 68 | PF00069 | 0.528 |
DOC_MAPK_MEF2A_6 | 61 | 70 | PF00069 | 0.516 |
DOC_PP4_FxxP_1 | 253 | 256 | PF00568 | 0.602 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 169 | 173 | PF00917 | 0.653 |
DOC_USP7_MATH_1 | 211 | 215 | PF00917 | 0.645 |
DOC_USP7_MATH_1 | 298 | 302 | PF00917 | 0.577 |
DOC_USP7_MATH_1 | 328 | 332 | PF00917 | 0.535 |
DOC_USP7_MATH_1 | 338 | 342 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 81 | 85 | PF00917 | 0.494 |
DOC_USP7_UBL2_3 | 5 | 9 | PF12436 | 0.645 |
DOC_WW_Pin1_4 | 146 | 151 | PF00397 | 0.738 |
DOC_WW_Pin1_4 | 42 | 47 | PF00397 | 0.559 |
DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.653 |
LIG_14-3-3_CanoR_1 | 273 | 283 | PF00244 | 0.664 |
LIG_14-3-3_CanoR_1 | 357 | 363 | PF00244 | 0.653 |
LIG_BIR_III_4 | 367 | 371 | PF00653 | 0.603 |
LIG_FHA_1 | 12 | 18 | PF00498 | 0.636 |
LIG_FHA_1 | 191 | 197 | PF00498 | 0.711 |
LIG_FHA_1 | 22 | 28 | PF00498 | 0.448 |
LIG_FHA_1 | 224 | 230 | PF00498 | 0.616 |
LIG_FHA_2 | 243 | 249 | PF00498 | 0.626 |
LIG_FHA_2 | 273 | 279 | PF00498 | 0.656 |
LIG_FHA_2 | 362 | 368 | PF00498 | 0.659 |
LIG_FHA_2 | 377 | 383 | PF00498 | 0.532 |
LIG_LIR_Apic_2 | 250 | 256 | PF02991 | 0.611 |
LIG_LIR_Apic_2 | 282 | 286 | PF02991 | 0.650 |
LIG_LIR_Gen_1 | 293 | 302 | PF02991 | 0.498 |
LIG_LIR_Gen_1 | 315 | 324 | PF02991 | 0.507 |
LIG_LIR_Gen_1 | 84 | 92 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 293 | 297 | PF02991 | 0.545 |
LIG_LIR_Nem_3 | 315 | 320 | PF02991 | 0.548 |
LIG_LIR_Nem_3 | 84 | 88 | PF02991 | 0.458 |
LIG_NRBOX | 379 | 385 | PF00104 | 0.649 |
LIG_SH2_CRK | 317 | 321 | PF00017 | 0.609 |
LIG_SH2_NCK_1 | 121 | 125 | PF00017 | 0.636 |
LIG_SH2_NCK_1 | 78 | 82 | PF00017 | 0.378 |
LIG_SH2_STAP1 | 121 | 125 | PF00017 | 0.636 |
LIG_SH2_STAT3 | 281 | 284 | PF00017 | 0.664 |
LIG_SH2_STAT5 | 152 | 155 | PF00017 | 0.624 |
LIG_SH2_STAT5 | 91 | 94 | PF00017 | 0.518 |
LIG_SH3_2 | 102 | 107 | PF14604 | 0.690 |
LIG_SH3_3 | 202 | 208 | PF00018 | 0.689 |
LIG_SH3_3 | 396 | 402 | PF00018 | 0.641 |
LIG_SH3_3 | 99 | 105 | PF00018 | 0.785 |
LIG_SH3_4 | 5 | 12 | PF00018 | 0.643 |
LIG_SUMO_SIM_anti_2 | 379 | 387 | PF11976 | 0.648 |
LIG_SUMO_SIM_par_1 | 220 | 226 | PF11976 | 0.527 |
LIG_SUMO_SIM_par_1 | 376 | 382 | PF11976 | 0.595 |
LIG_TRAF2_1 | 268 | 271 | PF00917 | 0.597 |
LIG_TRAF2_1 | 343 | 346 | PF00917 | 0.551 |
LIG_TYR_ITIM | 89 | 94 | PF00017 | 0.512 |
MOD_CDK_SPxK_1 | 101 | 107 | PF00069 | 0.686 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.646 |
MOD_CK1_1 | 176 | 182 | PF00069 | 0.667 |
MOD_CK1_1 | 190 | 196 | PF00069 | 0.583 |
MOD_CK1_1 | 203 | 209 | PF00069 | 0.602 |
MOD_CK2_1 | 287 | 293 | PF00069 | 0.589 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.617 |
MOD_GlcNHglycan | 167 | 170 | PF01048 | 0.625 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.661 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.617 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.661 |
MOD_GlcNHglycan | 213 | 216 | PF01048 | 0.565 |
MOD_GlcNHglycan | 310 | 314 | PF01048 | 0.583 |
MOD_GlcNHglycan | 394 | 399 | PF01048 | 0.672 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.648 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.670 |
MOD_GSK3_1 | 187 | 194 | PF00069 | 0.727 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.670 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.510 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.614 |
MOD_N-GLC_1 | 203 | 208 | PF02516 | 0.657 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.635 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.593 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.611 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.530 |
MOD_NEK2_2 | 328 | 333 | PF00069 | 0.527 |
MOD_PIKK_1 | 251 | 257 | PF00454 | 0.650 |
MOD_PIKK_1 | 338 | 344 | PF00454 | 0.545 |
MOD_PIKK_1 | 44 | 50 | PF00454 | 0.535 |
MOD_PKA_2 | 272 | 278 | PF00069 | 0.652 |
MOD_PKA_2 | 322 | 328 | PF00069 | 0.630 |
MOD_Plk_1 | 163 | 169 | PF00069 | 0.713 |
MOD_Plk_1 | 62 | 68 | PF00069 | 0.581 |
MOD_Plk_2-3 | 272 | 278 | PF00069 | 0.652 |
MOD_Plk_4 | 13 | 19 | PF00069 | 0.668 |
MOD_Plk_4 | 298 | 304 | PF00069 | 0.553 |
MOD_Plk_4 | 376 | 382 | PF00069 | 0.652 |
MOD_ProDKin_1 | 146 | 152 | PF00069 | 0.741 |
MOD_ProDKin_1 | 42 | 48 | PF00069 | 0.563 |
MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.661 |
MOD_SUMO_for_1 | 183 | 186 | PF00179 | 0.694 |
MOD_SUMO_rev_2 | 162 | 167 | PF00179 | 0.754 |
TRG_DiLeu_BaEn_4 | 271 | 277 | PF01217 | 0.624 |
TRG_ENDOCYTIC_2 | 317 | 320 | PF00928 | 0.551 |
TRG_ENDOCYTIC_2 | 91 | 94 | PF00928 | 0.518 |
TRG_ER_diArg_1 | 332 | 335 | PF00400 | 0.594 |
TRG_ER_diArg_1 | 56 | 58 | PF00400 | 0.538 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7X275 | Leishmania donovani | 94% | 100% |
A4HH43 | Leishmania braziliensis | 69% | 98% |
A4I496 | Leishmania infantum | 94% | 100% |
E9AM37 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |