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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: E9B2C4
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 6 |
GO:0043167 | ion binding | 2 | 5 |
GO:0043169 | cation binding | 3 | 5 |
GO:0046872 | metal ion binding | 4 | 5 |
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 | 313 | 317 | PF00656 | 0.502 |
CLV_MEL_PAP_1 | 100 | 106 | PF00089 | 0.422 |
CLV_NRD_NRD_1 | 121 | 123 | PF00675 | 0.451 |
CLV_NRD_NRD_1 | 164 | 166 | PF00675 | 0.544 |
CLV_NRD_NRD_1 | 253 | 255 | PF00675 | 0.785 |
CLV_NRD_NRD_1 | 59 | 61 | PF00675 | 0.466 |
CLV_NRD_NRD_1 | 68 | 70 | PF00675 | 0.481 |
CLV_NRD_NRD_1 | 84 | 86 | PF00675 | 0.403 |
CLV_PCSK_KEX2_1 | 121 | 123 | PF00082 | 0.486 |
CLV_PCSK_KEX2_1 | 253 | 255 | PF00082 | 0.622 |
CLV_PCSK_KEX2_1 | 68 | 70 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 84 | 86 | PF00082 | 0.405 |
CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 21 | 25 | PF00082 | 0.529 |
CLV_PCSK_SKI1_1 | 233 | 237 | PF00082 | 0.723 |
CLV_PCSK_SKI1_1 | 68 | 72 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 73 | 77 | PF00082 | 0.451 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 93 | 97 | PF00082 | 0.261 |
DEG_COP1_1 | 190 | 198 | PF00400 | 0.559 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.556 |
DEG_SCF_TRCP1_1 | 316 | 322 | PF00400 | 0.502 |
DOC_CYCLIN_RxL_1 | 119 | 129 | PF00134 | 0.495 |
DOC_CYCLIN_yCln2_LP_2 | 198 | 201 | PF00134 | 0.474 |
DOC_MAPK_gen_1 | 18 | 28 | PF00069 | 0.518 |
DOC_MAPK_MEF2A_6 | 18 | 26 | PF00069 | 0.484 |
DOC_PP2B_LxvP_1 | 198 | 201 | PF13499 | 0.549 |
DOC_USP7_MATH_1 | 189 | 193 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 301 | 305 | PF00917 | 0.591 |
DOC_WW_Pin1_4 | 77 | 82 | PF00397 | 0.448 |
LIG_14-3-3_CanoR_1 | 103 | 109 | PF00244 | 0.585 |
LIG_14-3-3_CanoR_1 | 60 | 66 | PF00244 | 0.379 |
LIG_APCC_ABBAyCdc20_2 | 121 | 127 | PF00400 | 0.476 |
LIG_BRCT_BRCA1_1 | 104 | 108 | PF00533 | 0.446 |
LIG_FHA_1 | 134 | 140 | PF00498 | 0.455 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.618 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.759 |
LIG_FHA_1 | 300 | 306 | PF00498 | 0.584 |
LIG_FHA_1 | 70 | 76 | PF00498 | 0.461 |
LIG_FHA_2 | 127 | 133 | PF00498 | 0.544 |
LIG_FHA_2 | 307 | 313 | PF00498 | 0.507 |
LIG_LIR_Nem_3 | 211 | 217 | PF02991 | 0.701 |
LIG_MYND_1 | 196 | 200 | PF01753 | 0.636 |
LIG_NRBOX | 82 | 88 | PF00104 | 0.492 |
LIG_Pex14_2 | 28 | 32 | PF04695 | 0.471 |
LIG_REV1ctd_RIR_1 | 68 | 77 | PF16727 | 0.480 |
LIG_SH2_CRK | 214 | 218 | PF00017 | 0.769 |
LIG_SH2_NCK_1 | 116 | 120 | PF00017 | 0.437 |
LIG_SH2_NCK_1 | 63 | 67 | PF00017 | 0.496 |
LIG_SH2_SRC | 159 | 162 | PF00017 | 0.448 |
LIG_SH2_STAP1 | 116 | 120 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 159 | 162 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 63 | 66 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 99 | 102 | PF00017 | 0.387 |
LIG_SH3_2 | 228 | 233 | PF14604 | 0.573 |
LIG_SH3_3 | 198 | 204 | PF00018 | 0.685 |
LIG_SH3_3 | 225 | 231 | PF00018 | 0.576 |
LIG_SUMO_SIM_anti_2 | 135 | 141 | PF11976 | 0.440 |
LIG_SUMO_SIM_par_1 | 208 | 213 | PF11976 | 0.479 |
LIG_TYR_ITIM | 212 | 217 | PF00017 | 0.613 |
LIG_UBA3_1 | 86 | 93 | PF00899 | 0.509 |
LIG_WRC_WIRS_1 | 29 | 34 | PF05994 | 0.480 |
MOD_CDK_SPxxK_3 | 77 | 84 | PF00069 | 0.447 |
MOD_CK1_1 | 126 | 132 | PF00069 | 0.535 |
MOD_CK1_1 | 135 | 141 | PF00069 | 0.467 |
MOD_CK1_1 | 150 | 156 | PF00069 | 0.494 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.530 |
MOD_CK1_1 | 264 | 270 | PF00069 | 0.774 |
MOD_CK1_1 | 283 | 289 | PF00069 | 0.504 |
MOD_CK1_1 | 292 | 298 | PF00069 | 0.702 |
MOD_CK1_1 | 310 | 316 | PF00069 | 0.622 |
MOD_CK1_1 | 336 | 342 | PF00069 | 0.744 |
MOD_CK2_1 | 126 | 132 | PF00069 | 0.609 |
MOD_CK2_1 | 301 | 307 | PF00069 | 0.737 |
MOD_CK2_1 | 319 | 325 | PF00069 | 0.640 |
MOD_Cter_Amidation | 251 | 254 | PF01082 | 0.605 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.257 |
MOD_GlcNHglycan | 127 | 132 | PF01048 | 0.464 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.807 |
MOD_GlcNHglycan | 228 | 231 | PF01048 | 0.638 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.735 |
MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.543 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.586 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.702 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.367 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.483 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.732 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.713 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.754 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.566 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.640 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.523 |
MOD_LATS_1 | 260 | 266 | PF00433 | 0.699 |
MOD_N-GLC_1 | 273 | 278 | PF02516 | 0.693 |
MOD_N-GLC_1 | 320 | 325 | PF02516 | 0.807 |
MOD_N-GLC_1 | 331 | 336 | PF02516 | 0.572 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.436 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.477 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.423 |
MOD_NEK2_2 | 189 | 194 | PF00069 | 0.553 |
MOD_PIKK_1 | 182 | 188 | PF00454 | 0.530 |
MOD_PIKK_1 | 283 | 289 | PF00454 | 0.641 |
MOD_PIKK_1 | 296 | 302 | PF00454 | 0.797 |
MOD_PKA_2 | 102 | 108 | PF00069 | 0.508 |
MOD_PKA_2 | 261 | 267 | PF00069 | 0.698 |
MOD_PKA_2 | 37 | 43 | PF00069 | 0.521 |
MOD_Plk_1 | 210 | 216 | PF00069 | 0.653 |
MOD_Plk_1 | 273 | 279 | PF00069 | 0.619 |
MOD_Plk_1 | 306 | 312 | PF00069 | 0.702 |
MOD_Plk_2-3 | 307 | 313 | PF00069 | 0.796 |
MOD_Plk_4 | 280 | 286 | PF00069 | 0.667 |
MOD_ProDKin_1 | 77 | 83 | PF00069 | 0.443 |
MOD_SUMO_rev_2 | 17 | 23 | PF00179 | 0.347 |
MOD_SUMO_rev_2 | 307 | 315 | PF00179 | 0.620 |
TRG_DiLeu_BaEn_1 | 82 | 87 | PF01217 | 0.513 |
TRG_DiLeu_LyEn_5 | 19 | 24 | PF01217 | 0.539 |
TRG_DiLeu_LyEn_5 | 82 | 87 | PF01217 | 0.450 |
TRG_ENDOCYTIC_2 | 214 | 217 | PF00928 | 0.758 |
TRG_ER_diArg_1 | 120 | 122 | PF00400 | 0.482 |
TRG_ER_diArg_1 | 253 | 255 | PF00400 | 0.802 |
TRG_ER_diArg_1 | 68 | 70 | PF00400 | 0.536 |
TRG_ER_diArg_1 | 83 | 85 | PF00400 | 0.405 |
TRG_Pf-PMV_PEXEL_1 | 122 | 127 | PF00026 | 0.479 |
TRG_Pf-PMV_PEXEL_1 | 176 | 180 | PF00026 | 0.491 |
TRG_Pf-PMV_PEXEL_1 | 253 | 258 | PF00026 | 0.530 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2H1 | Leptomonas seymouri | 38% | 95% |
A0A0N1I963 | Leptomonas seymouri | 56% | 90% |
A0A3S7X526 | Leishmania donovani | 86% | 100% |
A4HJY4 | Leishmania braziliensis | 68% | 100% |
A4I7G7 | Leishmania infantum | 87% | 100% |
Q4Q5T2 | Leishmania major | 86% | 100% |