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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A4IBR3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 260 | 262 | PF00675 | 0.543 |
CLV_NRD_NRD_1 | 288 | 290 | PF00675 | 0.579 |
CLV_NRD_NRD_1 | 77 | 79 | PF00675 | 0.471 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.495 |
CLV_NRD_NRD_1 | 92 | 94 | PF00675 | 0.523 |
CLV_NRD_NRD_1 | 95 | 97 | PF00675 | 0.465 |
CLV_PCSK_FUR_1 | 89 | 93 | PF00082 | 0.543 |
CLV_PCSK_KEX2_1 | 260 | 262 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 288 | 290 | PF00082 | 0.486 |
CLV_PCSK_KEX2_1 | 76 | 78 | PF00082 | 0.489 |
CLV_PCSK_KEX2_1 | 88 | 90 | PF00082 | 0.462 |
CLV_PCSK_KEX2_1 | 91 | 93 | PF00082 | 0.477 |
CLV_PCSK_KEX2_1 | 95 | 97 | PF00082 | 0.414 |
CLV_PCSK_PC1ET2_1 | 76 | 78 | PF00082 | 0.532 |
CLV_PCSK_PC1ET2_1 | 91 | 93 | PF00082 | 0.384 |
CLV_PCSK_PC7_1 | 284 | 290 | PF00082 | 0.601 |
CLV_PCSK_PC7_1 | 88 | 94 | PF00082 | 0.551 |
CLV_PCSK_SKI1_1 | 78 | 82 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 96 | 100 | PF00082 | 0.438 |
DEG_APCC_DBOX_1 | 260 | 268 | PF00400 | 0.528 |
DEG_SCF_FBW7_1 | 56 | 63 | PF00400 | 0.635 |
DEG_SCF_FBW7_2 | 337 | 342 | PF00400 | 0.573 |
DEG_SPOP_SBC_1 | 22 | 26 | PF00917 | 0.472 |
DOC_CDC14_PxL_1 | 192 | 200 | PF14671 | 0.470 |
DOC_CYCLIN_yCln2_LP_2 | 272 | 278 | PF00134 | 0.519 |
DOC_PP1_RVXF_1 | 186 | 193 | PF00149 | 0.388 |
DOC_PP2B_LxvP_1 | 245 | 248 | PF13499 | 0.540 |
DOC_PP2B_LxvP_1 | 358 | 361 | PF13499 | 0.482 |
DOC_PP4_FxxP_1 | 172 | 175 | PF00568 | 0.423 |
DOC_PP4_FxxP_1 | 376 | 379 | PF00568 | 0.417 |
DOC_USP7_MATH_1 | 221 | 225 | PF00917 | 0.701 |
DOC_USP7_MATH_1 | 306 | 310 | PF00917 | 0.713 |
DOC_USP7_MATH_1 | 35 | 39 | PF00917 | 0.526 |
DOC_USP7_MATH_1 | 40 | 44 | PF00917 | 0.589 |
DOC_USP7_UBL2_3 | 57 | 61 | PF12436 | 0.603 |
DOC_WW_Pin1_4 | 238 | 243 | PF00397 | 0.459 |
DOC_WW_Pin1_4 | 335 | 340 | PF00397 | 0.545 |
DOC_WW_Pin1_4 | 375 | 380 | PF00397 | 0.440 |
DOC_WW_Pin1_4 | 56 | 61 | PF00397 | 0.636 |
LIG_14-3-3_CanoR_1 | 132 | 142 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 253 | 259 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 365 | 371 | PF00244 | 0.498 |
LIG_14-3-3_CanoR_1 | 42 | 47 | PF00244 | 0.570 |
LIG_APCC_ABBAyCdc20_2 | 188 | 194 | PF00400 | 0.384 |
LIG_BRCT_BRCA1_1 | 42 | 46 | PF00533 | 0.463 |
LIG_deltaCOP1_diTrp_1 | 270 | 276 | PF00928 | 0.601 |
LIG_DLG_GKlike_1 | 42 | 49 | PF00625 | 0.629 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.529 |
LIG_FHA_1 | 133 | 139 | PF00498 | 0.555 |
LIG_FHA_1 | 319 | 325 | PF00498 | 0.451 |
LIG_FHA_1 | 61 | 67 | PF00498 | 0.629 |
LIG_FHA_2 | 367 | 373 | PF00498 | 0.533 |
LIG_HCF-1_HBM_1 | 13 | 16 | PF13415 | 0.475 |
LIG_Integrin_isoDGR_2 | 103 | 105 | PF01839 | 0.516 |
LIG_LIR_Apic_2 | 170 | 175 | PF02991 | 0.445 |
LIG_LIR_Apic_2 | 200 | 205 | PF02991 | 0.463 |
LIG_LIR_Apic_2 | 373 | 379 | PF02991 | 0.420 |
LIG_LIR_Gen_1 | 13 | 23 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 43 | 52 | PF02991 | 0.582 |
LIG_LIR_Nem_3 | 13 | 19 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 270 | 276 | PF02991 | 0.585 |
LIG_LIR_Nem_3 | 43 | 49 | PF02991 | 0.573 |
LIG_PCNA_PIPBox_1 | 67 | 76 | PF02747 | 0.537 |
LIG_PCNA_yPIPBox_3 | 152 | 166 | PF02747 | 0.473 |
LIG_SH2_CRK | 16 | 20 | PF00017 | 0.398 |
LIG_SH2_CRK | 202 | 206 | PF00017 | 0.452 |
LIG_SH2_CRK | 208 | 212 | PF00017 | 0.411 |
LIG_SH2_NCK_1 | 16 | 20 | PF00017 | 0.503 |
LIG_SH2_SRC | 16 | 19 | PF00017 | 0.519 |
LIG_SH2_SRC | 263 | 266 | PF00017 | 0.583 |
LIG_SH2_STAT5 | 240 | 243 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 263 | 266 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 79 | 82 | PF00017 | 0.482 |
LIG_SH3_3 | 183 | 189 | PF00018 | 0.439 |
LIG_SH3_3 | 272 | 278 | PF00018 | 0.519 |
LIG_SH3_3 | 294 | 300 | PF00018 | 0.440 |
LIG_SH3_3 | 309 | 315 | PF00018 | 0.685 |
LIG_SH3_3 | 321 | 327 | PF00018 | 0.294 |
LIG_SH3_3 | 377 | 383 | PF00018 | 0.389 |
LIG_SH3_4 | 174 | 181 | PF00018 | 0.515 |
LIG_SUMO_SIM_anti_2 | 321 | 326 | PF11976 | 0.418 |
LIG_SUMO_SIM_par_1 | 320 | 326 | PF11976 | 0.424 |
LIG_TYR_ITIM | 206 | 211 | PF00017 | 0.546 |
LIG_UBA3_1 | 70 | 76 | PF00899 | 0.629 |
LIG_WRPW_2 | 273 | 276 | PF00400 | 0.647 |
LIG_WW_1 | 383 | 386 | PF00397 | 0.441 |
MOD_CDK_SPK_2 | 56 | 61 | PF00069 | 0.636 |
MOD_CK1_1 | 123 | 129 | PF00069 | 0.550 |
MOD_CK2_1 | 23 | 29 | PF00069 | 0.481 |
MOD_CK2_1 | 366 | 372 | PF00069 | 0.452 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.532 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.689 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.530 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.476 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.597 |
MOD_GSK3_1 | 236 | 243 | PF00069 | 0.476 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.445 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.582 |
MOD_N-GLC_1 | 335 | 340 | PF02516 | 0.424 |
MOD_NEK2_1 | 23 | 28 | PF00069 | 0.551 |
MOD_NEK2_1 | 252 | 257 | PF00069 | 0.456 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.445 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.459 |
MOD_NEK2_1 | 55 | 60 | PF00069 | 0.676 |
MOD_NEK2_2 | 134 | 139 | PF00069 | 0.527 |
MOD_NEK2_2 | 263 | 268 | PF00069 | 0.581 |
MOD_PIKK_1 | 123 | 129 | PF00454 | 0.567 |
MOD_PIKK_1 | 174 | 180 | PF00454 | 0.511 |
MOD_PIKK_1 | 252 | 258 | PF00454 | 0.470 |
MOD_PKA_2 | 221 | 227 | PF00069 | 0.675 |
MOD_PKA_2 | 252 | 258 | PF00069 | 0.489 |
MOD_Plk_1 | 228 | 234 | PF00069 | 0.579 |
MOD_Plk_1 | 292 | 298 | PF00069 | 0.445 |
MOD_Plk_4 | 23 | 29 | PF00069 | 0.454 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.375 |
MOD_Plk_4 | 292 | 298 | PF00069 | 0.445 |
MOD_Plk_4 | 318 | 324 | PF00069 | 0.394 |
MOD_Plk_4 | 359 | 365 | PF00069 | 0.413 |
MOD_Plk_4 | 51 | 57 | PF00069 | 0.556 |
MOD_ProDKin_1 | 238 | 244 | PF00069 | 0.469 |
MOD_ProDKin_1 | 335 | 341 | PF00069 | 0.545 |
MOD_ProDKin_1 | 375 | 381 | PF00069 | 0.434 |
MOD_ProDKin_1 | 56 | 62 | PF00069 | 0.638 |
TRG_DiLeu_BaLyEn_6 | 193 | 198 | PF01217 | 0.497 |
TRG_DiLeu_BaLyEn_6 | 297 | 302 | PF01217 | 0.492 |
TRG_ENDOCYTIC_2 | 16 | 19 | PF00928 | 0.377 |
TRG_ENDOCYTIC_2 | 208 | 211 | PF00928 | 0.544 |
TRG_ENDOCYTIC_2 | 84 | 87 | PF00928 | 0.591 |
TRG_ER_diArg_1 | 259 | 261 | PF00400 | 0.526 |
TRG_ER_diArg_1 | 287 | 289 | PF00400 | 0.595 |
TRG_ER_diArg_1 | 77 | 79 | PF00400 | 0.521 |
TRG_ER_diArg_1 | 87 | 89 | PF00400 | 0.495 |
TRG_ER_diArg_1 | 92 | 95 | PF00400 | 0.486 |
TRG_NLS_Bipartite_1 | 76 | 95 | PF00514 | 0.530 |
TRG_NLS_MonoExtC_3 | 90 | 95 | PF00514 | 0.585 |
TRG_NLS_MonoExtN_4 | 88 | 95 | PF00514 | 0.542 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCF2 | Leptomonas seymouri | 71% | 100% |
A0A0S4J0E9 | Bodo saltans | 32% | 96% |
A0A1X0P564 | Trypanosomatidae | 46% | 100% |
A0A3Q8IJC4 | Leishmania donovani | 100% | 100% |
A0A3R7R9I8 | Trypanosoma rangeli | 47% | 100% |
A4HN45 | Leishmania braziliensis | 87% | 100% |
C9ZYW0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 100% |
E9AFJ8 | Leishmania major | 96% | 100% |
E9B6Q2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
V5BCU7 | Trypanosoma cruzi | 47% | 100% |