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: A4H899
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 220 | 224 | PF00656 | 0.461 |
CLV_C14_Caspase3-7 | 270 | 274 | PF00656 | 0.607 |
CLV_NRD_NRD_1 | 178 | 180 | PF00675 | 0.718 |
CLV_NRD_NRD_1 | 55 | 57 | PF00675 | 0.461 |
CLV_PCSK_KEX2_1 | 178 | 180 | PF00082 | 0.710 |
CLV_PCSK_SKI1_1 | 207 | 211 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 60 | 64 | PF00082 | 0.606 |
DOC_CKS1_1 | 17 | 22 | PF01111 | 0.713 |
DOC_PP1_SILK_1 | 163 | 168 | PF00149 | 0.548 |
DOC_PP2B_LxvP_1 | 15 | 18 | PF13499 | 0.558 |
DOC_PP4_FxxP_1 | 189 | 192 | PF00568 | 0.566 |
DOC_USP7_MATH_1 | 132 | 136 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 90 | 94 | PF00917 | 0.580 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.644 |
DOC_WW_Pin1_4 | 113 | 118 | PF00397 | 0.754 |
DOC_WW_Pin1_4 | 121 | 126 | PF00397 | 0.780 |
DOC_WW_Pin1_4 | 16 | 21 | PF00397 | 0.484 |
DOC_WW_Pin1_4 | 194 | 199 | PF00397 | 0.808 |
DOC_WW_Pin1_4 | 236 | 241 | PF00397 | 0.506 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.802 |
LIG_14-3-3_CanoR_1 | 141 | 151 | PF00244 | 0.485 |
LIG_14-3-3_CanoR_1 | 194 | 198 | PF00244 | 0.668 |
LIG_14-3-3_CanoR_1 | 200 | 205 | PF00244 | 0.632 |
LIG_14-3-3_CanoR_1 | 207 | 217 | PF00244 | 0.590 |
LIG_14-3-3_CanoR_1 | 54 | 64 | PF00244 | 0.411 |
LIG_BIR_III_4 | 127 | 131 | PF00653 | 0.545 |
LIG_FHA_1 | 17 | 23 | PF00498 | 0.812 |
LIG_FHA_1 | 209 | 215 | PF00498 | 0.631 |
LIG_FHA_1 | 233 | 239 | PF00498 | 0.509 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.466 |
LIG_FHA_2 | 122 | 128 | PF00498 | 0.676 |
LIG_FHA_2 | 178 | 184 | PF00498 | 0.554 |
LIG_FHA_2 | 323 | 329 | PF00498 | 0.527 |
LIG_FHA_2 | 56 | 62 | PF00498 | 0.561 |
LIG_LIR_Apic_2 | 186 | 192 | PF02991 | 0.565 |
LIG_MYND_1 | 121 | 125 | PF01753 | 0.712 |
LIG_RPA_C_Fungi | 216 | 228 | PF08784 | 0.576 |
LIG_SH2_STAP1 | 301 | 305 | PF00017 | 0.667 |
LIG_SH2_STAT5 | 301 | 304 | PF00017 | 0.513 |
LIG_SH3_3 | 11 | 17 | PF00018 | 0.718 |
LIG_SH3_3 | 155 | 161 | PF00018 | 0.652 |
LIG_SH3_3 | 199 | 205 | PF00018 | 0.768 |
LIG_SH3_3 | 25 | 31 | PF00018 | 0.709 |
LIG_SUMO_SIM_par_1 | 234 | 239 | PF11976 | 0.490 |
LIG_TRAF2_1 | 281 | 284 | PF00917 | 0.829 |
LIG_UBA3_1 | 52 | 57 | PF00899 | 0.398 |
LIG_WW_2 | 20 | 23 | PF00397 | 0.717 |
LIG_WW_3 | 197 | 201 | PF00397 | 0.727 |
LIG_WW_3 | 204 | 208 | PF00397 | 0.742 |
MOD_CDC14_SPxK_1 | 197 | 200 | PF00782 | 0.561 |
MOD_CDC14_SPxK_1 | 6 | 9 | PF00782 | 0.566 |
MOD_CDK_SPxK_1 | 194 | 200 | PF00069 | 0.562 |
MOD_CDK_SPxK_1 | 3 | 9 | PF00069 | 0.566 |
MOD_CK1_1 | 168 | 174 | PF00069 | 0.712 |
MOD_CK1_1 | 177 | 183 | PF00069 | 0.739 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.570 |
MOD_CK1_1 | 250 | 256 | PF00069 | 0.651 |
MOD_CK1_1 | 296 | 302 | PF00069 | 0.624 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.749 |
MOD_CK1_1 | 309 | 315 | PF00069 | 0.599 |
MOD_CK2_1 | 142 | 148 | PF00069 | 0.629 |
MOD_CK2_1 | 177 | 183 | PF00069 | 0.553 |
MOD_CK2_1 | 322 | 328 | PF00069 | 0.527 |
MOD_CK2_1 | 55 | 61 | PF00069 | 0.561 |
MOD_Cter_Amidation | 172 | 175 | PF01082 | 0.590 |
MOD_DYRK1A_RPxSP_1 | 194 | 198 | PF00069 | 0.560 |
MOD_GlcNHglycan | 133 | 137 | PF01048 | 0.561 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.644 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.818 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.692 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.773 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.756 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.788 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.681 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.672 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.645 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.728 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.498 |
MOD_NEK2_1 | 187 | 192 | PF00069 | 0.566 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.627 |
MOD_NEK2_1 | 293 | 298 | PF00069 | 0.583 |
MOD_NEK2_1 | 55 | 60 | PF00069 | 0.489 |
MOD_PKA_1 | 174 | 180 | PF00069 | 0.553 |
MOD_PKA_2 | 177 | 183 | PF00069 | 0.757 |
MOD_PKA_2 | 193 | 199 | PF00069 | 0.714 |
MOD_PKA_2 | 307 | 313 | PF00069 | 0.571 |
MOD_PKA_2 | 55 | 61 | PF00069 | 0.480 |
MOD_Plk_1 | 90 | 96 | PF00069 | 0.509 |
MOD_Plk_4 | 161 | 167 | PF00069 | 0.542 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.639 |
MOD_ProDKin_1 | 113 | 119 | PF00069 | 0.755 |
MOD_ProDKin_1 | 121 | 127 | PF00069 | 0.780 |
MOD_ProDKin_1 | 194 | 200 | PF00069 | 0.809 |
MOD_ProDKin_1 | 236 | 242 | PF00069 | 0.508 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.804 |
TRG_DiLeu_BaLyEn_6 | 48 | 53 | PF01217 | 0.633 |
TRG_ER_diArg_1 | 53 | 56 | PF00400 | 0.556 |
TRG_NES_CRM1_1 | 137 | 150 | PF08389 | 0.479 |
TRG_NLS_MonoExtC_3 | 173 | 178 | PF00514 | 0.639 |
TRG_NLS_MonoExtN_4 | 174 | 179 | PF00514 | 0.616 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEC2 | Leptomonas seymouri | 37% | 96% |
A0A3Q8IDH2 | Leishmania donovani | 62% | 100% |
A4HWM1 | Leishmania infantum | 61% | 100% |
E9AQC8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 62% | 100% |
Q4QF47 | Leishmania major | 58% | 99% |