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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A4H3F2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 103 | 107 | PF00656 | 0.530 |
CLV_NRD_NRD_1 | 136 | 138 | PF00675 | 0.477 |
CLV_NRD_NRD_1 | 150 | 152 | PF00675 | 0.373 |
CLV_NRD_NRD_1 | 187 | 189 | PF00675 | 0.706 |
CLV_NRD_NRD_1 | 308 | 310 | PF00675 | 0.601 |
CLV_NRD_NRD_1 | 33 | 35 | PF00675 | 0.423 |
CLV_PCSK_KEX2_1 | 11 | 13 | PF00082 | 0.510 |
CLV_PCSK_KEX2_1 | 136 | 138 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 150 | 152 | PF00082 | 0.414 |
CLV_PCSK_KEX2_1 | 187 | 189 | PF00082 | 0.684 |
CLV_PCSK_KEX2_1 | 310 | 312 | PF00082 | 0.579 |
CLV_PCSK_PC1ET2_1 | 11 | 13 | PF00082 | 0.510 |
CLV_PCSK_PC1ET2_1 | 310 | 312 | PF00082 | 0.574 |
CLV_PCSK_SKI1_1 | 102 | 106 | PF00082 | 0.564 |
CLV_PCSK_SKI1_1 | 311 | 315 | PF00082 | 0.621 |
CLV_PCSK_SKI1_1 | 35 | 39 | PF00082 | 0.410 |
DEG_APCC_DBOX_1 | 135 | 143 | PF00400 | 0.442 |
DEG_APCC_DBOX_1 | 285 | 293 | PF00400 | 0.485 |
DOC_CKS1_1 | 195 | 200 | PF01111 | 0.671 |
DOC_PP2B_LxvP_1 | 232 | 235 | PF13499 | 0.485 |
DOC_USP7_MATH_1 | 222 | 226 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 227 | 231 | PF00917 | 0.568 |
DOC_USP7_MATH_1 | 263 | 267 | PF00917 | 0.653 |
DOC_USP7_UBL2_3 | 31 | 35 | PF12436 | 0.525 |
DOC_WW_Pin1_4 | 194 | 199 | PF00397 | 0.605 |
LIG_14-3-3_CanoR_1 | 12 | 20 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 136 | 140 | PF00244 | 0.441 |
LIG_14-3-3_CanoR_1 | 188 | 198 | PF00244 | 0.772 |
LIG_14-3-3_CanoR_1 | 261 | 268 | PF00244 | 0.524 |
LIG_14-3-3_CanoR_1 | 296 | 301 | PF00244 | 0.606 |
LIG_14-3-3_CanoR_1 | 34 | 38 | PF00244 | 0.319 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.428 |
LIG_Clathr_ClatBox_1 | 164 | 168 | PF01394 | 0.350 |
LIG_FHA_1 | 8 | 14 | PF00498 | 0.450 |
LIG_FHA_2 | 55 | 61 | PF00498 | 0.565 |
LIG_FHA_2 | 74 | 80 | PF00498 | 0.310 |
LIG_LIR_Apic_2 | 299 | 303 | PF02991 | 0.691 |
LIG_LIR_Gen_1 | 92 | 101 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 92 | 97 | PF02991 | 0.518 |
LIG_PTB_Apo_2 | 93 | 100 | PF02174 | 0.462 |
LIG_SH2_CRK | 300 | 304 | PF00017 | 0.691 |
LIG_SH2_GRB2like | 94 | 97 | PF00017 | 0.466 |
LIG_SH2_SRC | 44 | 47 | PF00017 | 0.522 |
LIG_SH2_STAP1 | 44 | 48 | PF00017 | 0.408 |
LIG_SH3_1 | 300 | 306 | PF00018 | 0.571 |
LIG_SH3_3 | 195 | 201 | PF00018 | 0.663 |
LIG_SH3_3 | 246 | 252 | PF00018 | 0.556 |
LIG_SH3_3 | 300 | 306 | PF00018 | 0.546 |
LIG_TRAF2_1 | 129 | 132 | PF00917 | 0.414 |
LIG_TRAF2_1 | 16 | 19 | PF00917 | 0.540 |
LIG_TRAF2_1 | 206 | 209 | PF00917 | 0.688 |
MOD_CDK_SPK_2 | 197 | 202 | PF00069 | 0.717 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.546 |
MOD_CK1_1 | 200 | 206 | PF00069 | 0.502 |
MOD_CK1_1 | 237 | 243 | PF00069 | 0.694 |
MOD_CK1_1 | 266 | 272 | PF00069 | 0.629 |
MOD_CK2_1 | 11 | 17 | PF00069 | 0.529 |
MOD_CK2_1 | 18 | 24 | PF00069 | 0.550 |
MOD_CK2_1 | 54 | 60 | PF00069 | 0.545 |
MOD_CK2_1 | 73 | 79 | PF00069 | 0.303 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.642 |
MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.694 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.666 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.627 |
MOD_GlcNHglycan | 270 | 273 | PF01048 | 0.644 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.587 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.622 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.614 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.434 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.387 |
MOD_NEK2_1 | 314 | 319 | PF00069 | 0.539 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.432 |
MOD_PIKK_1 | 144 | 150 | PF00454 | 0.447 |
MOD_PIKK_1 | 261 | 267 | PF00454 | 0.590 |
MOD_PKA_1 | 11 | 17 | PF00069 | 0.529 |
MOD_PKA_2 | 11 | 17 | PF00069 | 0.529 |
MOD_PKA_2 | 122 | 128 | PF00069 | 0.484 |
MOD_PKA_2 | 135 | 141 | PF00069 | 0.498 |
MOD_PKA_2 | 190 | 196 | PF00069 | 0.578 |
MOD_PKA_2 | 285 | 291 | PF00069 | 0.556 |
MOD_PKA_2 | 33 | 39 | PF00069 | 0.431 |
MOD_Plk_1 | 18 | 24 | PF00069 | 0.354 |
MOD_Plk_1 | 73 | 79 | PF00069 | 0.517 |
MOD_Plk_2-3 | 75 | 81 | PF00069 | 0.324 |
MOD_Plk_4 | 122 | 128 | PF00069 | 0.377 |
MOD_Plk_4 | 200 | 206 | PF00069 | 0.493 |
MOD_Plk_4 | 263 | 269 | PF00069 | 0.585 |
MOD_ProDKin_1 | 194 | 200 | PF00069 | 0.606 |
TRG_DiLeu_BaEn_1 | 51 | 56 | PF01217 | 0.469 |
TRG_DiLeu_BaEn_2 | 207 | 213 | PF01217 | 0.681 |
TRG_DiLeu_BaEn_2 | 94 | 100 | PF01217 | 0.463 |
TRG_DiLeu_BaEn_4 | 130 | 136 | PF01217 | 0.443 |
TRG_ENDOCYTIC_2 | 44 | 47 | PF00928 | 0.409 |
TRG_ENDOCYTIC_2 | 94 | 97 | PF00928 | 0.390 |
TRG_ER_diArg_1 | 135 | 137 | PF00400 | 0.547 |
TRG_ER_diArg_1 | 187 | 189 | PF00400 | 0.736 |
TRG_Pf-PMV_PEXEL_1 | 102 | 106 | PF00026 | 0.530 |
TRG_Pf-PMV_PEXEL_1 | 137 | 141 | PF00026 | 0.555 |
TRG_Pf-PMV_PEXEL_1 | 158 | 163 | PF00026 | 0.561 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HT89 | Leptomonas seymouri | 62% | 98% |
A0A1X0NQ36 | Trypanosomatidae | 37% | 93% |
A0A3R7LN24 | Trypanosoma rangeli | 40% | 95% |
A0A3S5H510 | Leishmania donovani | 85% | 100% |
A4HRQ6 | Leishmania infantum | 85% | 100% |
C9ZUN5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 94% |
E9ACD5 | Leishmania major | 86% | 100% |
E9AJM3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
V5DPV7 | Trypanosoma cruzi | 39% | 94% |