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: A0A3Q8IH36
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 109 | 113 | PF00656 | 0.449 |
CLV_C14_Caspase3-7 | 242 | 246 | PF00656 | 0.604 |
CLV_PCSK_SKI1_1 | 192 | 196 | PF00082 | 0.605 |
CLV_PCSK_SKI1_1 | 201 | 205 | PF00082 | 0.547 |
CLV_PCSK_SKI1_1 | 265 | 269 | PF00082 | 0.572 |
CLV_PCSK_SKI1_1 | 30 | 34 | PF00082 | 0.591 |
CLV_PCSK_SKI1_1 | 53 | 57 | PF00082 | 0.565 |
DEG_APCC_DBOX_1 | 191 | 199 | PF00400 | 0.593 |
DEG_SPOP_SBC_1 | 126 | 130 | PF00917 | 0.545 |
DOC_CYCLIN_RxL_1 | 189 | 199 | PF00134 | 0.595 |
DOC_CYCLIN_yCln2_LP_2 | 204 | 210 | PF00134 | 0.582 |
DOC_MAPK_HePTP_8 | 90 | 102 | PF00069 | 0.520 |
DOC_MAPK_MEF2A_6 | 251 | 260 | PF00069 | 0.487 |
DOC_MAPK_MEF2A_6 | 84 | 92 | PF00069 | 0.514 |
DOC_MAPK_MEF2A_6 | 93 | 102 | PF00069 | 0.510 |
DOC_PP2B_LxvP_1 | 184 | 187 | PF13499 | 0.565 |
DOC_PP2B_PxIxI_1 | 97 | 103 | PF00149 | 0.517 |
DOC_PP4_FxxP_1 | 74 | 77 | PF00568 | 0.539 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.538 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.453 |
DOC_USP7_MATH_1 | 140 | 144 | PF00917 | 0.515 |
DOC_USP7_MATH_1 | 176 | 180 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.645 |
DOC_USP7_MATH_1 | 237 | 241 | PF00917 | 0.493 |
DOC_USP7_MATH_1 | 306 | 310 | PF00917 | 0.581 |
DOC_USP7_MATH_1 | 48 | 52 | PF00917 | 0.747 |
DOC_WW_Pin1_4 | 203 | 208 | PF00397 | 0.629 |
DOC_WW_Pin1_4 | 209 | 214 | PF00397 | 0.646 |
DOC_WW_Pin1_4 | 219 | 224 | PF00397 | 0.666 |
DOC_WW_Pin1_4 | 44 | 49 | PF00397 | 0.584 |
LIG_14-3-3_CanoR_1 | 124 | 133 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 177 | 187 | PF00244 | 0.602 |
LIG_14-3-3_CanoR_1 | 295 | 302 | PF00244 | 0.628 |
LIG_14-3-3_CanoR_1 | 53 | 58 | PF00244 | 0.560 |
LIG_14-3-3_CanoR_1 | 7 | 13 | PF00244 | 0.594 |
LIG_14-3-3_CterR_2 | 383 | 385 | PF00244 | 0.632 |
LIG_Actin_WH2_2 | 187 | 203 | PF00022 | 0.622 |
LIG_Actin_WH2_2 | 340 | 355 | PF00022 | 0.465 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.608 |
LIG_BIR_III_2 | 45 | 49 | PF00653 | 0.583 |
LIG_BRCT_BRCA1_1 | 129 | 133 | PF00533 | 0.545 |
LIG_deltaCOP1_diTrp_1 | 280 | 283 | PF00928 | 0.457 |
LIG_FHA_1 | 147 | 153 | PF00498 | 0.538 |
LIG_FHA_1 | 179 | 185 | PF00498 | 0.678 |
LIG_FHA_1 | 58 | 64 | PF00498 | 0.483 |
LIG_FHA_1 | 77 | 83 | PF00498 | 0.452 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.392 |
LIG_FHA_2 | 286 | 292 | PF00498 | 0.513 |
LIG_FHA_2 | 357 | 363 | PF00498 | 0.508 |
LIG_FHA_2 | 366 | 372 | PF00498 | 0.552 |
LIG_FHA_2 | 54 | 60 | PF00498 | 0.477 |
LIG_FHA_2 | 89 | 95 | PF00498 | 0.508 |
LIG_LIR_Apic_2 | 280 | 284 | PF02991 | 0.497 |
LIG_LIR_Apic_2 | 71 | 77 | PF02991 | 0.538 |
LIG_LIR_Gen_1 | 101 | 111 | PF02991 | 0.535 |
LIG_LIR_Gen_1 | 362 | 372 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 101 | 107 | PF02991 | 0.543 |
LIG_LIR_Nem_3 | 2 | 8 | PF02991 | 0.616 |
LIG_LIR_Nem_3 | 280 | 286 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 362 | 367 | PF02991 | 0.558 |
LIG_Pex14_2 | 40 | 44 | PF04695 | 0.611 |
LIG_SH2_CRK | 104 | 108 | PF00017 | 0.523 |
LIG_SH3_2 | 210 | 215 | PF14604 | 0.579 |
LIG_SH3_3 | 204 | 210 | PF00018 | 0.624 |
LIG_SH3_3 | 217 | 223 | PF00018 | 0.634 |
LIG_SH3_3 | 335 | 341 | PF00018 | 0.557 |
LIG_SUMO_SIM_anti_2 | 334 | 340 | PF11976 | 0.567 |
LIG_SUMO_SIM_par_1 | 147 | 154 | PF11976 | 0.567 |
LIG_TYR_ITIM | 102 | 107 | PF00017 | 0.508 |
LIG_WRC_WIRS_1 | 1 | 6 | PF05994 | 0.558 |
LIG_WRC_WIRS_1 | 361 | 366 | PF05994 | 0.494 |
MOD_CDC14_SPxK_1 | 212 | 215 | PF00782 | 0.583 |
MOD_CDK_SPxK_1 | 209 | 215 | PF00069 | 0.576 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.554 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.628 |
MOD_CK1_1 | 222 | 228 | PF00069 | 0.674 |
MOD_CK1_1 | 301 | 307 | PF00069 | 0.637 |
MOD_CK1_1 | 355 | 361 | PF00069 | 0.502 |
MOD_CK1_1 | 47 | 53 | PF00069 | 0.631 |
MOD_CK2_1 | 113 | 119 | PF00069 | 0.539 |
MOD_CK2_1 | 163 | 169 | PF00069 | 0.636 |
MOD_CK2_1 | 285 | 291 | PF00069 | 0.499 |
MOD_CK2_1 | 356 | 362 | PF00069 | 0.482 |
MOD_CK2_1 | 365 | 371 | PF00069 | 0.508 |
MOD_CK2_1 | 53 | 59 | PF00069 | 0.494 |
MOD_CK2_1 | 88 | 94 | PF00069 | 0.512 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.552 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.591 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.639 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.499 |
MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.638 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.560 |
MOD_GlcNHglycan | 49 | 53 | PF01048 | 0.707 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.535 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.530 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.662 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.625 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.682 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.498 |
MOD_GSK3_1 | 351 | 358 | PF00069 | 0.488 |
MOD_GSK3_1 | 362 | 369 | PF00069 | 0.551 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.594 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.454 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.512 |
MOD_N-GLC_1 | 19 | 24 | PF02516 | 0.641 |
MOD_NEK2_1 | 127 | 132 | PF00069 | 0.591 |
MOD_NEK2_1 | 151 | 156 | PF00069 | 0.544 |
MOD_NEK2_1 | 256 | 261 | PF00069 | 0.442 |
MOD_NEK2_1 | 352 | 357 | PF00069 | 0.539 |
MOD_PIKK_1 | 132 | 138 | PF00454 | 0.555 |
MOD_PIKK_1 | 19 | 25 | PF00454 | 0.589 |
MOD_PIKK_1 | 295 | 301 | PF00454 | 0.639 |
MOD_PIKK_1 | 76 | 82 | PF00454 | 0.565 |
MOD_PKA_2 | 176 | 182 | PF00069 | 0.622 |
MOD_PKA_2 | 286 | 292 | PF00069 | 0.554 |
MOD_PKA_2 | 92 | 98 | PF00069 | 0.510 |
MOD_Plk_1 | 25 | 31 | PF00069 | 0.670 |
MOD_Plk_1 | 265 | 271 | PF00069 | 0.584 |
MOD_Plk_1 | 333 | 339 | PF00069 | 0.580 |
MOD_Plk_4 | 146 | 152 | PF00069 | 0.559 |
MOD_Plk_4 | 333 | 339 | PF00069 | 0.580 |
MOD_ProDKin_1 | 203 | 209 | PF00069 | 0.629 |
MOD_ProDKin_1 | 219 | 225 | PF00069 | 0.663 |
MOD_ProDKin_1 | 44 | 50 | PF00069 | 0.584 |
TRG_DiLeu_BaEn_1 | 110 | 115 | PF01217 | 0.540 |
TRG_DiLeu_BaLyEn_6 | 258 | 263 | PF01217 | 0.476 |
TRG_DiLeu_BaLyEn_6 | 289 | 294 | PF01217 | 0.535 |
TRG_ENDOCYTIC_2 | 104 | 107 | PF00928 | 0.537 |
TRG_ER_diArg_1 | 294 | 297 | PF00400 | 0.584 |
TRG_NES_CRM1_1 | 80 | 94 | PF08389 | 0.508 |
TRG_Pf-PMV_PEXEL_1 | 192 | 196 | PF00026 | 0.592 |
TRG_Pf-PMV_PEXEL_1 | 261 | 266 | PF00026 | 0.574 |
TRG_Pf-PMV_PEXEL_1 | 276 | 280 | PF00026 | 0.402 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HWJ1 | Leptomonas seymouri | 51% | 79% |
A4HAN3 | Leishmania braziliensis | 78% | 98% |
A4I9S5 | Leishmania infantum | 100% | 100% |
E9B4T6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 98% |
Q4Q390 | Leishmania major | 95% | 100% |