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: A4HQK7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 245 | 249 | PF00656 | 0.731 |
CLV_NRD_NRD_1 | 16 | 18 | PF00675 | 0.658 |
CLV_NRD_NRD_1 | 221 | 223 | PF00675 | 0.608 |
CLV_NRD_NRD_1 | 299 | 301 | PF00675 | 0.435 |
CLV_PCSK_KEX2_1 | 188 | 190 | PF00082 | 0.723 |
CLV_PCSK_KEX2_1 | 221 | 223 | PF00082 | 0.608 |
CLV_PCSK_KEX2_1 | 298 | 300 | PF00082 | 0.461 |
CLV_PCSK_KEX2_1 | 305 | 307 | PF00082 | 0.602 |
CLV_PCSK_PC1ET2_1 | 188 | 190 | PF00082 | 0.723 |
CLV_PCSK_PC1ET2_1 | 305 | 307 | PF00082 | 0.625 |
CLV_PCSK_SKI1_1 | 147 | 151 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 17 | 21 | PF00082 | 0.681 |
CLV_PCSK_SKI1_1 | 221 | 225 | PF00082 | 0.763 |
CLV_PCSK_SKI1_1 | 28 | 32 | PF00082 | 0.738 |
CLV_PCSK_SKI1_1 | 351 | 355 | PF00082 | 0.631 |
DEG_APCC_DBOX_1 | 146 | 154 | PF00400 | 0.476 |
DEG_APCC_DBOX_1 | 297 | 305 | PF00400 | 0.367 |
DOC_CKS1_1 | 135 | 140 | PF01111 | 0.505 |
DOC_CKS1_1 | 50 | 55 | PF01111 | 0.554 |
DOC_MAPK_MEF2A_6 | 310 | 317 | PF00069 | 0.368 |
DOC_MAPK_MEF2A_6 | 330 | 338 | PF00069 | 0.588 |
DOC_MAPK_MEF2A_6 | 374 | 383 | PF00069 | 0.562 |
DOC_MAPK_NFAT4_5 | 310 | 318 | PF00069 | 0.369 |
DOC_PP1_RVXF_1 | 15 | 22 | PF00149 | 0.649 |
DOC_PP1_RVXF_1 | 187 | 194 | PF00149 | 0.551 |
DOC_PP1_RVXF_1 | 199 | 205 | PF00149 | 0.587 |
DOC_PP2B_LxvP_1 | 56 | 59 | PF13499 | 0.809 |
DOC_PP4_FxxP_1 | 21 | 24 | PF00568 | 0.556 |
DOC_PP4_FxxP_1 | 270 | 273 | PF00568 | 0.610 |
DOC_PP4_MxPP_1 | 156 | 159 | PF00568 | 0.463 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.550 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.603 |
DOC_USP7_MATH_1 | 63 | 67 | PF00917 | 0.561 |
DOC_WW_Pin1_4 | 117 | 122 | PF00397 | 0.772 |
DOC_WW_Pin1_4 | 134 | 139 | PF00397 | 0.434 |
DOC_WW_Pin1_4 | 269 | 274 | PF00397 | 0.614 |
DOC_WW_Pin1_4 | 31 | 36 | PF00397 | 0.749 |
DOC_WW_Pin1_4 | 344 | 349 | PF00397 | 0.400 |
DOC_WW_Pin1_4 | 387 | 392 | PF00397 | 0.656 |
DOC_WW_Pin1_4 | 409 | 414 | PF00397 | 0.737 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.521 |
DOC_WW_Pin1_4 | 9 | 14 | PF00397 | 0.800 |
DOC_WW_Pin1_4 | 94 | 99 | PF00397 | 0.570 |
LIG_14-3-3_CanoR_1 | 143 | 150 | PF00244 | 0.730 |
LIG_14-3-3_CanoR_1 | 17 | 22 | PF00244 | 0.657 |
LIG_14-3-3_CanoR_1 | 228 | 234 | PF00244 | 0.794 |
LIG_14-3-3_CanoR_1 | 396 | 406 | PF00244 | 0.532 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.800 |
LIG_BRCT_BRCA1_1 | 65 | 69 | PF00533 | 0.553 |
LIG_EVH1_1 | 49 | 53 | PF00568 | 0.551 |
LIG_EVH1_2 | 121 | 125 | PF00568 | 0.779 |
LIG_FHA_1 | 126 | 132 | PF00498 | 0.660 |
LIG_FHA_1 | 18 | 24 | PF00498 | 0.804 |
LIG_FHA_1 | 254 | 260 | PF00498 | 0.515 |
LIG_FHA_1 | 345 | 351 | PF00498 | 0.401 |
LIG_FHA_1 | 388 | 394 | PF00498 | 0.620 |
LIG_FHA_2 | 170 | 176 | PF00498 | 0.471 |
LIG_FHA_2 | 243 | 249 | PF00498 | 0.730 |
LIG_FHA_2 | 73 | 79 | PF00498 | 0.810 |
LIG_LIR_Apic_2 | 105 | 110 | PF02991 | 0.485 |
LIG_LIR_Apic_2 | 20 | 24 | PF02991 | 0.554 |
LIG_LIR_Gen_1 | 160 | 169 | PF02991 | 0.626 |
LIG_LIR_Gen_1 | 235 | 246 | PF02991 | 0.531 |
LIG_LIR_Nem_3 | 160 | 164 | PF02991 | 0.531 |
LIG_LIR_Nem_3 | 235 | 241 | PF02991 | 0.535 |
LIG_LIR_Nem_3 | 291 | 297 | PF02991 | 0.597 |
LIG_LIR_Nem_3 | 66 | 72 | PF02991 | 0.597 |
LIG_LYPXL_S_1 | 108 | 112 | PF13949 | 0.752 |
LIG_LYPXL_yS_3 | 109 | 112 | PF13949 | 0.761 |
LIG_PCNA_PIPBox_1 | 208 | 217 | PF02747 | 0.647 |
LIG_Pex14_1 | 265 | 269 | PF04695 | 0.578 |
LIG_SH2_CRK | 238 | 242 | PF00017 | 0.529 |
LIG_SH2_NCK_1 | 238 | 242 | PF00017 | 0.529 |
LIG_SH2_STAP1 | 104 | 108 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 161 | 164 | PF00017 | 0.520 |
LIG_SH2_STAT5 | 215 | 218 | PF00017 | 0.683 |
LIG_SH2_STAT5 | 238 | 241 | PF00017 | 0.537 |
LIG_SH2_STAT5 | 269 | 272 | PF00017 | 0.603 |
LIG_SH2_STAT5 | 294 | 297 | PF00017 | 0.596 |
LIG_SH3_3 | 1 | 7 | PF00018 | 0.743 |
LIG_SH3_3 | 127 | 133 | PF00018 | 0.527 |
LIG_SH3_3 | 174 | 180 | PF00018 | 0.705 |
LIG_SH3_3 | 33 | 39 | PF00018 | 0.648 |
LIG_SH3_3 | 362 | 368 | PF00018 | 0.610 |
LIG_SH3_3 | 40 | 46 | PF00018 | 0.653 |
LIG_SH3_3 | 47 | 53 | PF00018 | 0.687 |
LIG_SH3_3 | 56 | 62 | PF00018 | 0.534 |
LIG_SH3_3 | 92 | 98 | PF00018 | 0.557 |
LIG_SUMO_SIM_anti_2 | 170 | 178 | PF11976 | 0.522 |
LIG_SUMO_SIM_anti_2 | 332 | 340 | PF11976 | 0.453 |
LIG_SUMO_SIM_par_1 | 179 | 186 | PF11976 | 0.755 |
LIG_SUMO_SIM_par_1 | 332 | 340 | PF11976 | 0.453 |
LIG_SUMO_SIM_par_1 | 38 | 44 | PF11976 | 0.546 |
LIG_TRAF2_1 | 74 | 77 | PF00917 | 0.811 |
LIG_TRAF2_1 | 90 | 93 | PF00917 | 0.574 |
LIG_TRAF2_1 | 97 | 100 | PF00917 | 0.497 |
LIG_WW_1 | 158 | 161 | PF00397 | 0.689 |
MOD_CDK_SPK_2 | 344 | 349 | PF00069 | 0.400 |
MOD_CDK_SPxxK_3 | 117 | 124 | PF00069 | 0.525 |
MOD_CDK_SPxxK_3 | 344 | 351 | PF00069 | 0.399 |
MOD_CDK_SPxxK_3 | 409 | 416 | PF00069 | 0.535 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.668 |
MOD_CK1_1 | 12 | 18 | PF00069 | 0.571 |
MOD_CK1_1 | 170 | 176 | PF00069 | 0.574 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.774 |
MOD_CK1_1 | 253 | 259 | PF00069 | 0.507 |
MOD_CK1_1 | 355 | 361 | PF00069 | 0.629 |
MOD_CK1_1 | 387 | 393 | PF00069 | 0.572 |
MOD_CK2_1 | 142 | 148 | PF00069 | 0.591 |
MOD_CK2_1 | 72 | 78 | PF00069 | 0.814 |
MOD_CK2_1 | 87 | 93 | PF00069 | 0.574 |
MOD_CK2_1 | 94 | 100 | PF00069 | 0.478 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.628 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.567 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.326 |
MOD_GlcNHglycan | 339 | 342 | PF01048 | 0.562 |
MOD_GlcNHglycan | 354 | 357 | PF01048 | 0.394 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.768 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.532 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.784 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.403 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.642 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.700 |
MOD_LATS_1 | 375 | 381 | PF00433 | 0.561 |
MOD_NEK2_1 | 113 | 118 | PF00069 | 0.764 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.439 |
MOD_NEK2_1 | 337 | 342 | PF00069 | 0.494 |
MOD_NEK2_1 | 383 | 388 | PF00069 | 0.572 |
MOD_NEK2_1 | 394 | 399 | PF00069 | 0.695 |
MOD_PKA_1 | 17 | 23 | PF00069 | 0.806 |
MOD_PKA_1 | 221 | 227 | PF00069 | 0.617 |
MOD_PKA_2 | 142 | 148 | PF00069 | 0.738 |
MOD_PKA_2 | 221 | 227 | PF00069 | 0.722 |
MOD_PKA_2 | 317 | 323 | PF00069 | 0.329 |
MOD_PKA_2 | 342 | 348 | PF00069 | 0.543 |
MOD_PKA_2 | 415 | 421 | PF00069 | 0.524 |
MOD_Plk_1 | 394 | 400 | PF00069 | 0.533 |
MOD_Plk_4 | 152 | 158 | PF00069 | 0.474 |
MOD_Plk_4 | 17 | 23 | PF00069 | 0.556 |
MOD_Plk_4 | 317 | 323 | PF00069 | 0.429 |
MOD_Plk_4 | 79 | 85 | PF00069 | 0.567 |
MOD_ProDKin_1 | 117 | 123 | PF00069 | 0.773 |
MOD_ProDKin_1 | 134 | 140 | PF00069 | 0.432 |
MOD_ProDKin_1 | 269 | 275 | PF00069 | 0.613 |
MOD_ProDKin_1 | 31 | 37 | PF00069 | 0.751 |
MOD_ProDKin_1 | 344 | 350 | PF00069 | 0.394 |
MOD_ProDKin_1 | 387 | 393 | PF00069 | 0.656 |
MOD_ProDKin_1 | 409 | 415 | PF00069 | 0.736 |
MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.520 |
MOD_ProDKin_1 | 9 | 15 | PF00069 | 0.601 |
MOD_ProDKin_1 | 94 | 100 | PF00069 | 0.566 |
MOD_SUMO_for_1 | 216 | 219 | PF00179 | 0.647 |
MOD_SUMO_rev_2 | 90 | 96 | PF00179 | 0.571 |
TRG_ENDOCYTIC_2 | 109 | 112 | PF00928 | 0.636 |
TRG_ENDOCYTIC_2 | 161 | 164 | PF00928 | 0.553 |
TRG_ENDOCYTIC_2 | 215 | 218 | PF00928 | 0.674 |
TRG_ENDOCYTIC_2 | 238 | 241 | PF00928 | 0.534 |
TRG_ER_diArg_1 | 221 | 223 | PF00400 | 0.608 |
TRG_ER_diArg_1 | 297 | 300 | PF00400 | 0.426 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IGY1 | Leishmania donovani | 68% | 100% |
A4ICC7 | Leishmania infantum | 67% | 100% |
E9AUC2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 69% | 100% |
Q4Q068 | Leishmania major | 68% | 100% |