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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: Q4Q4R0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 188 | 192 | PF00656 | 0.417 |
CLV_NRD_NRD_1 | 51 | 53 | PF00675 | 0.543 |
CLV_PCSK_KEX2_1 | 51 | 53 | PF00082 | 0.543 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.500 |
DOC_CKS1_1 | 201 | 206 | PF01111 | 0.479 |
DOC_PP2B_LxvP_1 | 180 | 183 | PF13499 | 0.396 |
DOC_USP7_UBL2_3 | 190 | 194 | PF12436 | 0.460 |
DOC_WW_Pin1_4 | 200 | 205 | PF00397 | 0.542 |
DOC_WW_Pin1_4 | 214 | 219 | PF00397 | 0.364 |
DOC_WW_Pin1_4 | 43 | 48 | PF00397 | 0.708 |
DOC_WW_Pin1_4 | 72 | 77 | PF00397 | 0.722 |
DOC_WW_Pin1_4 | 78 | 83 | PF00397 | 0.621 |
DOC_WW_Pin1_4 | 87 | 92 | PF00397 | 0.581 |
LIG_14-3-3_CanoR_1 | 22 | 29 | PF00244 | 0.673 |
LIG_14-3-3_CanoR_1 | 51 | 61 | PF00244 | 0.589 |
LIG_BRCT_BRCA1_1 | 113 | 117 | PF00533 | 0.573 |
LIG_BRCT_BRCA1_1 | 120 | 124 | PF00533 | 0.409 |
LIG_deltaCOP1_diTrp_1 | 158 | 164 | PF00928 | 0.405 |
LIG_FHA_1 | 227 | 233 | PF00498 | 0.382 |
LIG_FHA_1 | 37 | 43 | PF00498 | 0.549 |
LIG_FHA_1 | 56 | 62 | PF00498 | 0.543 |
LIG_FHA_2 | 201 | 207 | PF00498 | 0.428 |
LIG_FHA_2 | 72 | 78 | PF00498 | 0.704 |
LIG_FHA_2 | 99 | 105 | PF00498 | 0.520 |
LIG_LIR_Apic_2 | 200 | 204 | PF02991 | 0.461 |
LIG_LIR_Apic_2 | 233 | 238 | PF02991 | 0.509 |
LIG_LIR_Gen_1 | 222 | 232 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 195 | 199 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 222 | 227 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 229 | 234 | PF02991 | 0.385 |
LIG_Pex14_1 | 160 | 164 | PF04695 | 0.469 |
LIG_SH2_NCK_1 | 54 | 58 | PF00017 | 0.593 |
LIG_SH2_PTP2 | 128 | 131 | PF00017 | 0.394 |
LIG_SH2_PTP2 | 231 | 234 | PF00017 | 0.467 |
LIG_SH2_STAP1 | 140 | 144 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 128 | 131 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 196 | 199 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 202 | 205 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 231 | 234 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.558 |
LIG_SH3_1 | 147 | 153 | PF00018 | 0.484 |
LIG_SH3_2 | 47 | 52 | PF14604 | 0.635 |
LIG_SH3_3 | 147 | 153 | PF00018 | 0.481 |
LIG_SH3_3 | 173 | 179 | PF00018 | 0.370 |
LIG_SH3_3 | 44 | 50 | PF00018 | 0.610 |
LIG_SH3_3 | 91 | 97 | PF00018 | 0.699 |
LIG_SUMO_SIM_par_1 | 178 | 185 | PF11976 | 0.399 |
LIG_TRAF2_1 | 3 | 6 | PF00917 | 0.571 |
LIG_WRC_WIRS_1 | 161 | 166 | PF05994 | 0.440 |
MOD_CDC14_SPxK_1 | 49 | 52 | PF00782 | 0.628 |
MOD_CDC14_SPxK_1 | 75 | 78 | PF00782 | 0.683 |
MOD_CDC14_SPxK_1 | 90 | 93 | PF00782 | 0.454 |
MOD_CDK_SPK_2 | 46 | 51 | PF00069 | 0.534 |
MOD_CDK_SPxK_1 | 46 | 52 | PF00069 | 0.626 |
MOD_CDK_SPxK_1 | 72 | 78 | PF00069 | 0.679 |
MOD_CDK_SPxK_1 | 87 | 93 | PF00069 | 0.467 |
MOD_CDK_SPxxK_3 | 214 | 221 | PF00069 | 0.454 |
MOD_CK1_1 | 166 | 172 | PF00069 | 0.429 |
MOD_CK1_1 | 46 | 52 | PF00069 | 0.651 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.669 |
MOD_CK1_1 | 67 | 73 | PF00069 | 0.791 |
MOD_CK2_1 | 139 | 145 | PF00069 | 0.566 |
MOD_CK2_1 | 200 | 206 | PF00069 | 0.419 |
MOD_CK2_1 | 214 | 220 | PF00069 | 0.371 |
MOD_CK2_1 | 98 | 104 | PF00069 | 0.548 |
MOD_DYRK1A_RPxSP_1 | 78 | 82 | PF00069 | 0.643 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.558 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.551 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.315 |
MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.637 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.684 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.754 |
MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.784 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.435 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.413 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.742 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.724 |
MOD_N-GLC_1 | 192 | 197 | PF02516 | 0.531 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.535 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.553 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.546 |
MOD_NEK2_1 | 256 | 261 | PF00069 | 0.655 |
MOD_PK_1 | 64 | 70 | PF00069 | 0.784 |
MOD_PKA_2 | 111 | 117 | PF00069 | 0.578 |
MOD_PKA_2 | 166 | 172 | PF00069 | 0.436 |
MOD_PKA_2 | 50 | 56 | PF00069 | 0.645 |
MOD_Plk_1 | 192 | 198 | PF00069 | 0.418 |
MOD_Plk_4 | 103 | 109 | PF00069 | 0.435 |
MOD_Plk_4 | 192 | 198 | PF00069 | 0.393 |
MOD_ProDKin_1 | 200 | 206 | PF00069 | 0.545 |
MOD_ProDKin_1 | 214 | 220 | PF00069 | 0.360 |
MOD_ProDKin_1 | 43 | 49 | PF00069 | 0.707 |
MOD_ProDKin_1 | 72 | 78 | PF00069 | 0.726 |
MOD_ProDKin_1 | 87 | 93 | PF00069 | 0.584 |
MOD_SUMO_rev_2 | 184 | 192 | PF00179 | 0.444 |
TRG_DiLeu_BaEn_1 | 223 | 228 | PF01217 | 0.491 |
TRG_DiLeu_BaEn_1 | 6 | 11 | PF01217 | 0.606 |
TRG_DiLeu_BaEn_4 | 6 | 12 | PF01217 | 0.551 |
TRG_DiLeu_BaLyEn_6 | 176 | 181 | PF01217 | 0.369 |
TRG_DiLeu_LyEn_5 | 6 | 11 | PF01217 | 0.567 |
TRG_ENDOCYTIC_2 | 128 | 131 | PF00928 | 0.394 |
TRG_ENDOCYTIC_2 | 196 | 199 | PF00928 | 0.387 |
TRG_ENDOCYTIC_2 | 231 | 234 | PF00928 | 0.467 |
TRG_ER_diArg_1 | 50 | 52 | PF00400 | 0.538 |
TRG_Pf-PMV_PEXEL_1 | 9 | 14 | PF00026 | 0.564 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBT8 | Leptomonas seymouri | 56% | 95% |
A0A3Q8IG98 | Leishmania donovani | 94% | 100% |
A0A3R7P3C4 | Trypanosoma rangeli | 49% | 100% |
A4HL01 | Leishmania braziliensis | 78% | 96% |
A4I8I2 | Leishmania infantum | 94% | 100% |
E9B3E2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |