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: A4H8X5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 124 | 128 | PF00656 | 0.542 |
CLV_NRD_NRD_1 | 187 | 189 | PF00675 | 0.701 |
CLV_NRD_NRD_1 | 280 | 282 | PF00675 | 0.506 |
CLV_NRD_NRD_1 | 41 | 43 | PF00675 | 0.443 |
CLV_PCSK_FUR_1 | 277 | 281 | PF00082 | 0.545 |
CLV_PCSK_FUR_1 | 45 | 49 | PF00082 | 0.509 |
CLV_PCSK_KEX2_1 | 211 | 213 | PF00082 | 0.640 |
CLV_PCSK_KEX2_1 | 277 | 279 | PF00082 | 0.559 |
CLV_PCSK_KEX2_1 | 280 | 282 | PF00082 | 0.501 |
CLV_PCSK_KEX2_1 | 47 | 49 | PF00082 | 0.433 |
CLV_PCSK_PC1ET2_1 | 211 | 213 | PF00082 | 0.545 |
CLV_PCSK_PC1ET2_1 | 47 | 49 | PF00082 | 0.506 |
CLV_PCSK_PC7_1 | 274 | 280 | PF00082 | 0.627 |
CLV_PCSK_SKI1_1 | 281 | 285 | PF00082 | 0.417 |
CLV_PCSK_SKI1_1 | 82 | 86 | PF00082 | 0.397 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.489 |
DEG_SCF_FBW7_1 | 19 | 26 | PF00400 | 0.387 |
DOC_CKS1_1 | 20 | 25 | PF01111 | 0.376 |
DOC_MAPK_gen_1 | 45 | 54 | PF00069 | 0.390 |
DOC_PP2B_LxvP_1 | 251 | 254 | PF13499 | 0.540 |
DOC_PP4_FxxP_1 | 162 | 165 | PF00568 | 0.495 |
DOC_SPAK_OSR1_1 | 30 | 34 | PF12202 | 0.364 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 180 | 184 | PF00917 | 0.530 |
DOC_USP7_UBL2_3 | 43 | 47 | PF12436 | 0.378 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.604 |
DOC_WW_Pin1_4 | 195 | 200 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 206 | 211 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 242 | 247 | PF00397 | 0.558 |
LIG_14-3-3_CanoR_1 | 147 | 151 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 181 | 185 | PF00244 | 0.565 |
LIG_14-3-3_CanoR_1 | 278 | 286 | PF00244 | 0.519 |
LIG_APCC_ABBA_1 | 119 | 124 | PF00400 | 0.411 |
LIG_BIR_III_4 | 127 | 131 | PF00653 | 0.494 |
LIG_FHA_1 | 20 | 26 | PF00498 | 0.378 |
LIG_LIR_Apic_2 | 161 | 165 | PF02991 | 0.495 |
LIG_LIR_Apic_2 | 175 | 180 | PF02991 | 0.492 |
LIG_LIR_Gen_1 | 29 | 35 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 29 | 34 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 291 | 297 | PF02991 | 0.436 |
LIG_MYND_1 | 250 | 254 | PF01753 | 0.511 |
LIG_Pex14_2 | 31 | 35 | PF04695 | 0.361 |
LIG_PTAP_UEV_1 | 150 | 155 | PF05743 | 0.489 |
LIG_SH2_CRK | 177 | 181 | PF00017 | 0.500 |
LIG_SH2_SRC | 60 | 63 | PF00017 | 0.260 |
LIG_SH2_STAP1 | 122 | 126 | PF00017 | 0.511 |
LIG_SH2_STAP1 | 56 | 60 | PF00017 | 0.281 |
LIG_SH2_STAT5 | 60 | 63 | PF00017 | 0.393 |
LIG_SH3_2 | 207 | 212 | PF14604 | 0.526 |
LIG_SH3_3 | 148 | 154 | PF00018 | 0.483 |
LIG_SH3_3 | 196 | 202 | PF00018 | 0.590 |
LIG_SH3_3 | 204 | 210 | PF00018 | 0.660 |
LIG_TRAF2_1 | 121 | 124 | PF00917 | 0.584 |
LIG_WRC_WIRS_1 | 159 | 164 | PF05994 | 0.496 |
MOD_CDC14_SPxK_1 | 209 | 212 | PF00782 | 0.537 |
MOD_CDK_SPK_2 | 206 | 211 | PF00069 | 0.525 |
MOD_CDK_SPxK_1 | 206 | 212 | PF00069 | 0.581 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.617 |
MOD_CK1_1 | 158 | 164 | PF00069 | 0.723 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.501 |
MOD_CK1_1 | 282 | 288 | PF00069 | 0.557 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.515 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.491 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.667 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.558 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.479 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.447 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.604 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.557 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.581 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.667 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.595 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.569 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.491 |
MOD_NEK2_1 | 145 | 150 | PF00069 | 0.472 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.496 |
MOD_NEK2_1 | 191 | 196 | PF00069 | 0.638 |
MOD_NEK2_1 | 237 | 242 | PF00069 | 0.559 |
MOD_PK_1 | 231 | 237 | PF00069 | 0.607 |
MOD_PKA_1 | 279 | 285 | PF00069 | 0.590 |
MOD_PKA_2 | 146 | 152 | PF00069 | 0.579 |
MOD_PKA_2 | 15 | 21 | PF00069 | 0.463 |
MOD_PKA_2 | 180 | 186 | PF00069 | 0.592 |
MOD_PKA_2 | 279 | 285 | PF00069 | 0.544 |
MOD_PKA_2 | 36 | 42 | PF00069 | 0.458 |
MOD_PKB_1 | 277 | 285 | PF00069 | 0.599 |
MOD_Plk_1 | 100 | 106 | PF00069 | 0.296 |
MOD_Plk_1 | 56 | 62 | PF00069 | 0.360 |
MOD_Plk_4 | 15 | 21 | PF00069 | 0.562 |
MOD_Plk_4 | 180 | 186 | PF00069 | 0.495 |
MOD_Plk_4 | 217 | 223 | PF00069 | 0.548 |
MOD_Plk_4 | 267 | 273 | PF00069 | 0.469 |
MOD_Plk_4 | 56 | 62 | PF00069 | 0.349 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.594 |
MOD_ProDKin_1 | 195 | 201 | PF00069 | 0.644 |
MOD_ProDKin_1 | 206 | 212 | PF00069 | 0.587 |
MOD_ProDKin_1 | 242 | 248 | PF00069 | 0.562 |
MOD_SUMO_for_1 | 46 | 49 | PF00179 | 0.506 |
TRG_DiLeu_BaEn_4 | 112 | 118 | PF01217 | 0.405 |
TRG_DiLeu_BaLyEn_6 | 247 | 252 | PF01217 | 0.517 |
TRG_ER_diArg_1 | 185 | 188 | PF00400 | 0.734 |
TRG_ER_diArg_1 | 277 | 280 | PF00400 | 0.549 |
TRG_NES_CRM1_1 | 108 | 123 | PF08389 | 0.340 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I9Y1 | Leptomonas seymouri | 38% | 93% |
A0A3S7WUB2 | Leishmania donovani | 62% | 90% |
A4HX99 | Leishmania infantum | 64% | 91% |
E9AR01 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 65% | 100% |
Q4QEG2 | Leishmania major | 64% | 100% |