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: 3 |
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: E9AMP4
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 7 |
GO:0003677 | DNA binding | 4 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 229 | 233 | PF00656 | 0.644 |
CLV_C14_Caspase3-7 | 255 | 259 | PF00656 | 0.521 |
CLV_C14_Caspase3-7 | 343 | 347 | PF00656 | 0.590 |
CLV_MEL_PAP_1 | 272 | 278 | PF00089 | 0.516 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.665 |
CLV_PCSK_FUR_1 | 205 | 209 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 14 | 16 | PF00082 | 0.312 |
CLV_PCSK_KEX2_1 | 207 | 209 | PF00082 | 0.665 |
CLV_PCSK_PC1ET2_1 | 14 | 16 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 136 | 140 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 325 | 329 | PF00082 | 0.728 |
CLV_PCSK_SKI1_1 | 360 | 364 | PF00082 | 0.678 |
CLV_PCSK_SKI1_1 | 42 | 46 | PF00082 | 0.312 |
DEG_APCC_DBOX_1 | 114 | 122 | PF00400 | 0.285 |
DEG_COP1_1 | 124 | 132 | PF00400 | 0.421 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.542 |
DEG_SCF_TRCP1_1 | 337 | 343 | PF00400 | 0.528 |
DEG_SPOP_SBC_1 | 352 | 356 | PF00917 | 0.639 |
DOC_CYCLIN_RxL_1 | 39 | 49 | PF00134 | 0.312 |
DOC_CYCLIN_yCln2_LP_2 | 219 | 222 | PF00134 | 0.601 |
DOC_CYCLIN_yCln2_LP_2 | 87 | 93 | PF00134 | 0.388 |
DOC_MAPK_MEF2A_6 | 122 | 129 | PF00069 | 0.476 |
DOC_PP2B_LxvP_1 | 127 | 130 | PF13499 | 0.489 |
DOC_PP2B_LxvP_1 | 219 | 222 | PF13499 | 0.601 |
DOC_PP2B_LxvP_1 | 328 | 331 | PF13499 | 0.529 |
DOC_PP2B_LxvP_1 | 45 | 48 | PF13499 | 0.312 |
DOC_PP2B_LxvP_1 | 453 | 456 | PF13499 | 0.312 |
DOC_PP2B_LxvP_1 | 85 | 88 | PF13499 | 0.312 |
DOC_USP7_MATH_1 | 16 | 20 | PF00917 | 0.416 |
DOC_USP7_MATH_1 | 212 | 216 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 263 | 267 | PF00917 | 0.671 |
DOC_USP7_MATH_1 | 304 | 308 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 342 | 346 | PF00917 | 0.745 |
LIG_14-3-3_CanoR_1 | 20 | 27 | PF00244 | 0.327 |
LIG_14-3-3_CanoR_1 | 207 | 212 | PF00244 | 0.604 |
LIG_14-3-3_CanoR_1 | 240 | 246 | PF00244 | 0.661 |
LIG_14-3-3_CanoR_1 | 325 | 331 | PF00244 | 0.588 |
LIG_14-3-3_CanoR_1 | 360 | 365 | PF00244 | 0.661 |
LIG_14-3-3_CanoR_1 | 465 | 474 | PF00244 | 0.341 |
LIG_14-3-3_CanoR_1 | 58 | 68 | PF00244 | 0.388 |
LIG_BIR_III_4 | 396 | 400 | PF00653 | 0.491 |
LIG_BRCT_BRCA1_1 | 468 | 472 | PF00533 | 0.255 |
LIG_BRCT_BRCA1_1 | 6 | 10 | PF00533 | 0.398 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.428 |
LIG_FHA_1 | 137 | 143 | PF00498 | 0.454 |
LIG_FHA_1 | 215 | 221 | PF00498 | 0.692 |
LIG_FHA_1 | 437 | 443 | PF00498 | 0.312 |
LIG_FHA_1 | 458 | 464 | PF00498 | 0.340 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.321 |
LIG_FHA_2 | 47 | 53 | PF00498 | 0.414 |
LIG_FHA_2 | 61 | 67 | PF00498 | 0.235 |
LIG_LIR_Gen_1 | 116 | 125 | PF02991 | 0.428 |
LIG_LIR_Gen_1 | 79 | 90 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 66 | 71 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 79 | 85 | PF02991 | 0.350 |
LIG_PDZ_Class_3 | 472 | 477 | PF00595 | 0.480 |
LIG_SH2_NCK_1 | 312 | 316 | PF00017 | 0.708 |
LIG_SH2_STAT5 | 415 | 418 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 54 | 57 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 82 | 85 | PF00017 | 0.312 |
LIG_SH3_3 | 388 | 394 | PF00018 | 0.498 |
LIG_SH3_3 | 453 | 459 | PF00018 | 0.501 |
LIG_SUMO_SIM_anti_2 | 439 | 444 | PF11976 | 0.312 |
MOD_CK1_1 | 105 | 111 | PF00069 | 0.312 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.584 |
MOD_CK1_1 | 19 | 25 | PF00069 | 0.388 |
MOD_CK1_1 | 214 | 220 | PF00069 | 0.604 |
MOD_CK1_1 | 307 | 313 | PF00069 | 0.742 |
MOD_CK1_1 | 457 | 463 | PF00069 | 0.366 |
MOD_CK1_1 | 466 | 472 | PF00069 | 0.317 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.312 |
MOD_CK2_1 | 105 | 111 | PF00069 | 0.312 |
MOD_CK2_1 | 299 | 305 | PF00069 | 0.708 |
MOD_CK2_1 | 315 | 321 | PF00069 | 0.537 |
MOD_CK2_1 | 46 | 52 | PF00069 | 0.418 |
MOD_CK2_1 | 60 | 66 | PF00069 | 0.237 |
MOD_GlcNHglycan | 156 | 159 | PF01048 | 0.637 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.584 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.725 |
MOD_GlcNHglycan | 241 | 244 | PF01048 | 0.636 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.571 |
MOD_GlcNHglycan | 258 | 262 | PF01048 | 0.704 |
MOD_GlcNHglycan | 305 | 309 | PF01048 | 0.684 |
MOD_GlcNHglycan | 337 | 340 | PF01048 | 0.720 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.312 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.312 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.312 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.606 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.599 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.610 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.663 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.722 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.724 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.674 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.330 |
MOD_N-GLC_1 | 105 | 110 | PF02516 | 0.312 |
MOD_N-GLC_1 | 30 | 35 | PF02516 | 0.340 |
MOD_NEK2_1 | 211 | 216 | PF00069 | 0.600 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.679 |
MOD_NEK2_1 | 351 | 356 | PF00069 | 0.721 |
MOD_OFUCOSY | 451 | 458 | PF10250 | 0.388 |
MOD_PIKK_1 | 212 | 218 | PF00454 | 0.644 |
MOD_PKA_1 | 207 | 213 | PF00069 | 0.662 |
MOD_PKA_2 | 19 | 25 | PF00069 | 0.312 |
MOD_PKA_2 | 207 | 213 | PF00069 | 0.600 |
MOD_PKA_2 | 239 | 245 | PF00069 | 0.735 |
MOD_PKB_1 | 149 | 157 | PF00069 | 0.601 |
MOD_PKB_1 | 205 | 213 | PF00069 | 0.609 |
MOD_Plk_1 | 105 | 111 | PF00069 | 0.312 |
MOD_Plk_1 | 30 | 36 | PF00069 | 0.340 |
MOD_Plk_1 | 4 | 10 | PF00069 | 0.410 |
MOD_Plk_2-3 | 226 | 232 | PF00069 | 0.506 |
MOD_Plk_4 | 214 | 220 | PF00069 | 0.622 |
MOD_Plk_4 | 307 | 313 | PF00069 | 0.712 |
MOD_Plk_4 | 353 | 359 | PF00069 | 0.686 |
MOD_Plk_4 | 436 | 442 | PF00069 | 0.312 |
TRG_DiLeu_BaLyEn_6 | 219 | 224 | PF01217 | 0.504 |
TRG_DiLeu_BaLyEn_6 | 403 | 408 | PF01217 | 0.457 |
TRG_ENDOCYTIC_2 | 68 | 71 | PF00928 | 0.339 |
TRG_ENDOCYTIC_2 | 82 | 85 | PF00928 | 0.312 |
TRG_ER_diArg_1 | 205 | 208 | PF00400 | 0.676 |
TRG_ER_diArg_1 | 404 | 407 | PF00400 | 0.477 |
TRG_Pf-PMV_PEXEL_1 | 406 | 411 | PF00026 | 0.444 |
TRG_Pf-PMV_PEXEL_1 | 42 | 46 | PF00026 | 0.312 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I698 | Leptomonas seymouri | 61% | 99% |
A0A3S5H6D0 | Leishmania donovani | 88% | 100% |
A4H5L9 | Leishmania braziliensis | 71% | 96% |
A4HTV7 | Leishmania infantum | 88% | 100% |
Q4QHY1 | Leishmania major | 88% | 98% |