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: 5 |
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: 5, no: 4 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: A4HMH1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 89 | 91 | PF00675 | 0.656 |
CLV_PCSK_SKI1_1 | 37 | 41 | PF00082 | 0.511 |
DEG_MDM2_SWIB_1 | 257 | 264 | PF02201 | 0.537 |
DEG_SPOP_SBC_1 | 220 | 224 | PF00917 | 0.455 |
DOC_MAPK_MEF2A_6 | 95 | 102 | PF00069 | 0.343 |
DOC_PP4_FxxP_1 | 164 | 167 | PF00568 | 0.596 |
DOC_PP4_FxxP_1 | 209 | 212 | PF00568 | 0.412 |
DOC_PP4_FxxP_1 | 70 | 73 | PF00568 | 0.514 |
DOC_PP4_FxxP_1 | 79 | 82 | PF00568 | 0.449 |
DOC_SPAK_OSR1_1 | 117 | 121 | PF12202 | 0.304 |
DOC_USP7_MATH_1 | 177 | 181 | PF00917 | 0.581 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.767 |
DOC_WW_Pin1_4 | 108 | 113 | PF00397 | 0.622 |
DOC_WW_Pin1_4 | 155 | 160 | PF00397 | 0.551 |
DOC_WW_Pin1_4 | 172 | 177 | PF00397 | 0.622 |
DOC_WW_Pin1_4 | 202 | 207 | PF00397 | 0.517 |
LIG_14-3-3_CanoR_1 | 23 | 31 | PF00244 | 0.519 |
LIG_14-3-3_CanoR_1 | 238 | 244 | PF00244 | 0.731 |
LIG_14-3-3_CanoR_1 | 84 | 94 | PF00244 | 0.602 |
LIG_Clathr_ClatBox_1 | 191 | 195 | PF01394 | 0.530 |
LIG_CtBP_PxDLS_1 | 248 | 252 | PF00389 | 0.424 |
LIG_eIF4E_1 | 108 | 114 | PF01652 | 0.587 |
LIG_FHA_1 | 109 | 115 | PF00498 | 0.569 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.544 |
LIG_FHA_1 | 214 | 220 | PF00498 | 0.572 |
LIG_FHA_1 | 244 | 250 | PF00498 | 0.699 |
LIG_FHA_1 | 25 | 31 | PF00498 | 0.506 |
LIG_FHA_1 | 251 | 257 | PF00498 | 0.480 |
LIG_LIR_Apic_2 | 207 | 212 | PF02991 | 0.440 |
LIG_LIR_Gen_1 | 186 | 197 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 115 | 121 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 158 | 164 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 186 | 192 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 193 | 199 | PF02991 | 0.416 |
LIG_PCNA_PIPBox_1 | 1 | 10 | PF02747 | 0.602 |
LIG_PDZ_Class_2 | 275 | 280 | PF00595 | 0.472 |
LIG_Pex14_1 | 185 | 189 | PF04695 | 0.650 |
LIG_Pex14_2 | 192 | 196 | PF04695 | 0.314 |
LIG_Pex14_2 | 257 | 261 | PF04695 | 0.606 |
LIG_SH2_NCK_1 | 156 | 160 | PF00017 | 0.636 |
LIG_SH2_SRC | 71 | 74 | PF00017 | 0.433 |
LIG_SH2_STAT3 | 22 | 25 | PF00017 | 0.566 |
LIG_SH2_STAT5 | 119 | 122 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 71 | 74 | PF00017 | 0.584 |
LIG_SH2_STAT5 | 8 | 11 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.506 |
LIG_SH3_3 | 170 | 176 | PF00018 | 0.514 |
LIG_SUMO_SIM_anti_2 | 246 | 253 | PF11976 | 0.433 |
LIG_SUMO_SIM_par_1 | 246 | 253 | PF11976 | 0.606 |
LIG_TRAF2_1 | 176 | 179 | PF00917 | 0.680 |
MOD_CDK_SPxxK_3 | 155 | 162 | PF00069 | 0.472 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.610 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.646 |
MOD_CK1_1 | 222 | 228 | PF00069 | 0.707 |
MOD_CK1_1 | 234 | 240 | PF00069 | 0.548 |
MOD_CK2_1 | 100 | 106 | PF00069 | 0.445 |
MOD_CK2_1 | 141 | 147 | PF00069 | 0.610 |
MOD_GlcNHglycan | 102 | 105 | PF01048 | 0.468 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.523 |
MOD_GlcNHglycan | 139 | 143 | PF01048 | 0.567 |
MOD_GlcNHglycan | 232 | 236 | PF01048 | 0.719 |
MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.550 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.675 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.371 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.654 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.685 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.593 |
MOD_N-GLC_1 | 121 | 126 | PF02516 | 0.459 |
MOD_N-GLC_1 | 265 | 270 | PF02516 | 0.679 |
MOD_N-GLC_1 | 56 | 61 | PF02516 | 0.689 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.558 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.683 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.523 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.545 |
MOD_PIKK_1 | 177 | 183 | PF00454 | 0.701 |
MOD_PIKK_1 | 61 | 67 | PF00454 | 0.434 |
MOD_PKA_2 | 100 | 106 | PF00069 | 0.295 |
MOD_PKA_2 | 239 | 245 | PF00069 | 0.571 |
MOD_PKA_2 | 25 | 31 | PF00069 | 0.529 |
MOD_PKA_2 | 83 | 89 | PF00069 | 0.617 |
MOD_Plk_4 | 25 | 31 | PF00069 | 0.413 |
MOD_Plk_4 | 89 | 95 | PF00069 | 0.505 |
MOD_ProDKin_1 | 108 | 114 | PF00069 | 0.611 |
MOD_ProDKin_1 | 155 | 161 | PF00069 | 0.551 |
MOD_ProDKin_1 | 172 | 178 | PF00069 | 0.623 |
MOD_ProDKin_1 | 202 | 208 | PF00069 | 0.509 |
TRG_DiLeu_BaEn_1 | 247 | 252 | PF01217 | 0.432 |
TRG_DiLeu_BaLyEn_6 | 109 | 114 | PF01217 | 0.383 |
TRG_ENDOCYTIC_2 | 189 | 192 | PF00928 | 0.502 |
TRG_NES_CRM1_1 | 183 | 195 | PF08389 | 0.386 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I5Y1 | Leptomonas seymouri | 52% | 77% |
A0A0S4JB49 | Bodo saltans | 28% | 92% |
A0A1X0P5P8 | Trypanosomatidae | 30% | 92% |
A0A3Q8IHV2 | Leishmania donovani | 74% | 99% |
A0A3R7LR32 | Trypanosoma rangeli | 34% | 92% |
A4IB51 | Leishmania infantum | 74% | 73% |
C9ZZF6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 89% |
E9B628 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 100% |