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: A4ICC7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 245 | 249 | PF00656 | 0.740 |
CLV_NRD_NRD_1 | 282 | 284 | PF00675 | 0.640 |
CLV_NRD_NRD_1 | 299 | 301 | PF00675 | 0.449 |
CLV_PCSK_KEX2_1 | 188 | 190 | PF00082 | 0.784 |
CLV_PCSK_KEX2_1 | 282 | 284 | PF00082 | 0.644 |
CLV_PCSK_KEX2_1 | 298 | 300 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 305 | 307 | PF00082 | 0.608 |
CLV_PCSK_PC1ET2_1 | 188 | 190 | PF00082 | 0.784 |
CLV_PCSK_PC1ET2_1 | 282 | 284 | PF00082 | 0.629 |
CLV_PCSK_PC1ET2_1 | 298 | 300 | PF00082 | 0.400 |
CLV_PCSK_PC1ET2_1 | 305 | 307 | PF00082 | 0.631 |
CLV_PCSK_SKI1_1 | 17 | 21 | PF00082 | 0.653 |
CLV_PCSK_SKI1_1 | 185 | 189 | PF00082 | 0.617 |
CLV_PCSK_SKI1_1 | 221 | 225 | PF00082 | 0.766 |
CLV_PCSK_SKI1_1 | 351 | 355 | PF00082 | 0.625 |
DEG_APCC_DBOX_1 | 410 | 418 | PF00400 | 0.713 |
DEG_SCF_FBW7_1 | 392 | 399 | PF00400 | 0.599 |
DOC_CKS1_1 | 393 | 398 | PF01111 | 0.601 |
DOC_MAPK_MEF2A_6 | 330 | 338 | PF00069 | 0.582 |
DOC_PP1_RVXF_1 | 15 | 22 | PF00149 | 0.622 |
DOC_PP1_RVXF_1 | 199 | 205 | PF00149 | 0.609 |
DOC_PP2B_LxvP_1 | 56 | 59 | PF13499 | 0.783 |
DOC_PP4_FxxP_1 | 270 | 273 | PF00568 | 0.608 |
DOC_USP7_MATH_1 | 384 | 388 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 397 | 401 | PF00917 | 0.559 |
DOC_WW_Pin1_4 | 117 | 122 | PF00397 | 0.772 |
DOC_WW_Pin1_4 | 269 | 274 | PF00397 | 0.606 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.754 |
DOC_WW_Pin1_4 | 31 | 36 | PF00397 | 0.723 |
DOC_WW_Pin1_4 | 317 | 322 | PF00397 | 0.519 |
DOC_WW_Pin1_4 | 392 | 397 | PF00397 | 0.667 |
DOC_WW_Pin1_4 | 409 | 414 | PF00397 | 0.737 |
DOC_WW_Pin1_4 | 63 | 68 | PF00397 | 0.726 |
DOC_WW_Pin1_4 | 9 | 14 | PF00397 | 0.698 |
LIG_14-3-3_CanoR_1 | 143 | 150 | PF00244 | 0.707 |
LIG_14-3-3_CanoR_1 | 178 | 184 | PF00244 | 0.653 |
LIG_14-3-3_CanoR_1 | 189 | 197 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 228 | 234 | PF00244 | 0.789 |
LIG_14-3-3_CanoR_1 | 73 | 80 | PF00244 | 0.734 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.798 |
LIG_EVH1_2 | 121 | 125 | PF00568 | 0.782 |
LIG_FHA_1 | 18 | 24 | PF00498 | 0.745 |
LIG_FHA_1 | 188 | 194 | PF00498 | 0.684 |
LIG_FHA_1 | 241 | 247 | PF00498 | 0.710 |
LIG_FHA_1 | 26 | 32 | PF00498 | 0.661 |
LIG_FHA_1 | 308 | 314 | PF00498 | 0.555 |
LIG_FHA_2 | 243 | 249 | PF00498 | 0.738 |
LIG_FHA_2 | 73 | 79 | PF00498 | 0.808 |
LIG_LIR_Gen_1 | 160 | 169 | PF02991 | 0.644 |
LIG_LIR_Nem_3 | 160 | 164 | PF02991 | 0.547 |
LIG_LIR_Nem_3 | 291 | 297 | PF02991 | 0.608 |
LIG_LIR_Nem_3 | 344 | 350 | PF02991 | 0.556 |
LIG_LYPXL_S_1 | 108 | 112 | PF13949 | 0.749 |
LIG_LYPXL_yS_3 | 109 | 112 | PF13949 | 0.749 |
LIG_MYND_1 | 39 | 43 | PF01753 | 0.649 |
LIG_PCNA_PIPBox_1 | 208 | 217 | PF02747 | 0.652 |
LIG_PDZ_Class_1 | 424 | 429 | PF00595 | 0.601 |
LIG_Pex14_1 | 265 | 269 | PF04695 | 0.583 |
LIG_SH2_CRK | 98 | 102 | PF00017 | 0.668 |
LIG_SH2_STAT5 | 161 | 164 | PF00017 | 0.537 |
LIG_SH2_STAT5 | 215 | 218 | PF00017 | 0.685 |
LIG_SH2_STAT5 | 269 | 272 | PF00017 | 0.605 |
LIG_SH2_STAT5 | 294 | 297 | PF00017 | 0.607 |
LIG_SH3_3 | 174 | 180 | PF00018 | 0.725 |
LIG_SH3_3 | 30 | 36 | PF00018 | 0.603 |
LIG_SH3_3 | 362 | 368 | PF00018 | 0.629 |
LIG_SH3_3 | 390 | 396 | PF00018 | 0.611 |
LIG_SH3_3 | 4 | 10 | PF00018 | 0.733 |
LIG_SH3_3 | 40 | 46 | PF00018 | 0.624 |
LIG_SH3_3 | 56 | 62 | PF00018 | 0.511 |
LIG_SH3_3 | 64 | 70 | PF00018 | 0.624 |
LIG_SUMO_SIM_anti_2 | 332 | 340 | PF11976 | 0.446 |
LIG_SUMO_SIM_par_1 | 179 | 184 | PF11976 | 0.775 |
LIG_SUMO_SIM_par_1 | 332 | 340 | PF11976 | 0.446 |
LIG_TRAF2_1 | 74 | 77 | PF00917 | 0.812 |
LIG_Vh1_VBS_1 | 324 | 342 | PF01044 | 0.520 |
LIG_WW_1 | 158 | 161 | PF00397 | 0.707 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.668 |
MOD_CK1_1 | 170 | 176 | PF00069 | 0.599 |
MOD_CK1_1 | 229 | 235 | PF00069 | 0.769 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.742 |
MOD_CK1_1 | 317 | 323 | PF00069 | 0.516 |
MOD_CK1_1 | 355 | 361 | PF00069 | 0.632 |
MOD_CK2_1 | 142 | 148 | PF00069 | 0.560 |
MOD_CK2_1 | 275 | 281 | PF00069 | 0.447 |
MOD_CK2_1 | 72 | 78 | PF00069 | 0.815 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.624 |
MOD_GlcNHglycan | 137 | 140 | PF01048 | 0.563 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.633 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.517 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.712 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.539 |
MOD_GlcNHglycan | 339 | 342 | PF01048 | 0.554 |
MOD_GlcNHglycan | 354 | 357 | PF01048 | 0.395 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.755 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.752 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.783 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.576 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.705 |
MOD_NEK2_1 | 113 | 118 | PF00069 | 0.748 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.714 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.711 |
MOD_NEK2_1 | 337 | 342 | PF00069 | 0.487 |
MOD_PK_1 | 330 | 336 | PF00069 | 0.456 |
MOD_PKA_1 | 17 | 23 | PF00069 | 0.781 |
MOD_PKA_1 | 188 | 194 | PF00069 | 0.634 |
MOD_PKA_2 | 142 | 148 | PF00069 | 0.708 |
MOD_PKA_2 | 167 | 173 | PF00069 | 0.537 |
MOD_PKA_2 | 188 | 194 | PF00069 | 0.756 |
MOD_PKA_2 | 227 | 233 | PF00069 | 0.736 |
MOD_PKA_2 | 342 | 348 | PF00069 | 0.531 |
MOD_PKA_2 | 72 | 78 | PF00069 | 0.740 |
MOD_Plk_1 | 343 | 349 | PF00069 | 0.464 |
MOD_Plk_4 | 275 | 281 | PF00069 | 0.424 |
MOD_Plk_4 | 307 | 313 | PF00069 | 0.604 |
MOD_Plk_4 | 330 | 336 | PF00069 | 0.525 |
MOD_Plk_4 | 361 | 367 | PF00069 | 0.575 |
MOD_ProDKin_1 | 117 | 123 | PF00069 | 0.773 |
MOD_ProDKin_1 | 269 | 275 | PF00069 | 0.608 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.753 |
MOD_ProDKin_1 | 31 | 37 | PF00069 | 0.726 |
MOD_ProDKin_1 | 317 | 323 | PF00069 | 0.516 |
MOD_ProDKin_1 | 392 | 398 | PF00069 | 0.670 |
MOD_ProDKin_1 | 409 | 415 | PF00069 | 0.738 |
MOD_ProDKin_1 | 63 | 69 | PF00069 | 0.728 |
MOD_SUMO_for_1 | 91 | 94 | PF00179 | 0.613 |
TRG_DiLeu_BaLyEn_6 | 67 | 72 | PF01217 | 0.731 |
TRG_ENDOCYTIC_2 | 109 | 112 | PF00928 | 0.624 |
TRG_ENDOCYTIC_2 | 161 | 164 | PF00928 | 0.569 |
TRG_ENDOCYTIC_2 | 215 | 218 | PF00928 | 0.676 |
TRG_ENDOCYTIC_2 | 98 | 101 | PF00928 | 0.633 |
TRG_NLS_Bipartite_1 | 282 | 302 | PF00514 | 0.472 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IGY1 | Leishmania donovani | 100% | 100% |
A4HQK7 | Leishmania braziliensis | 67% | 100% |
E9AUC2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4Q068 | Leishmania major | 86% | 100% |