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: A0A3Q8ID13
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 246 | 250 | PF00656 | 0.700 |
CLV_NRD_NRD_1 | 110 | 112 | PF00675 | 0.524 |
CLV_NRD_NRD_1 | 312 | 314 | PF00675 | 0.673 |
CLV_NRD_NRD_1 | 37 | 39 | PF00675 | 0.534 |
CLV_NRD_NRD_1 | 78 | 80 | PF00675 | 0.512 |
CLV_NRD_NRD_1 | 86 | 88 | PF00675 | 0.527 |
CLV_NRD_NRD_1 | 97 | 99 | PF00675 | 0.385 |
CLV_PCSK_FUR_1 | 310 | 314 | PF00082 | 0.623 |
CLV_PCSK_KEX2_1 | 312 | 314 | PF00082 | 0.673 |
CLV_PCSK_KEX2_1 | 37 | 39 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 78 | 80 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 86 | 88 | PF00082 | 0.517 |
CLV_PCSK_KEX2_1 | 97 | 99 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 160 | 164 | PF00082 | 0.731 |
CLV_PCSK_SKI1_1 | 79 | 83 | PF00082 | 0.508 |
CLV_PCSK_SKI1_1 | 87 | 91 | PF00082 | 0.485 |
DOC_MAPK_MEF2A_6 | 292 | 299 | PF00069 | 0.662 |
DOC_PP1_RVXF_1 | 5 | 11 | PF00149 | 0.667 |
DOC_PP2B_LxvP_1 | 322 | 325 | PF13499 | 0.608 |
DOC_USP7_MATH_1 | 201 | 205 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 220 | 224 | PF00917 | 0.424 |
DOC_USP7_MATH_1 | 236 | 240 | PF00917 | 0.739 |
LIG_14-3-3_CanoR_1 | 171 | 180 | PF00244 | 0.543 |
LIG_14-3-3_CanoR_1 | 203 | 210 | PF00244 | 0.679 |
LIG_14-3-3_CanoR_1 | 211 | 216 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 86 | 94 | PF00244 | 0.580 |
LIG_BIR_III_4 | 237 | 241 | PF00653 | 0.718 |
LIG_FHA_1 | 263 | 269 | PF00498 | 0.628 |
LIG_FHA_2 | 321 | 327 | PF00498 | 0.539 |
LIG_FHA_2 | 88 | 94 | PF00498 | 0.643 |
LIG_LIR_Nem_3 | 51 | 57 | PF02991 | 0.574 |
LIG_Pex14_1 | 170 | 174 | PF04695 | 0.732 |
LIG_SH2_CRK | 3 | 7 | PF00017 | 0.591 |
LIG_SH2_GRB2like | 16 | 19 | PF00017 | 0.642 |
LIG_SH2_SRC | 113 | 116 | PF00017 | 0.624 |
LIG_SH2_STAP1 | 16 | 20 | PF00017 | 0.634 |
LIG_SH2_STAT5 | 11 | 14 | PF00017 | 0.578 |
LIG_SH2_STAT5 | 147 | 150 | PF00017 | 0.561 |
LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.586 |
LIG_SH3_1 | 155 | 161 | PF00018 | 0.612 |
LIG_SH3_2 | 311 | 316 | PF14604 | 0.739 |
LIG_SH3_3 | 155 | 161 | PF00018 | 0.607 |
LIG_SH3_3 | 308 | 314 | PF00018 | 0.689 |
MOD_CK1_1 | 173 | 179 | PF00069 | 0.665 |
MOD_CK1_1 | 267 | 273 | PF00069 | 0.596 |
MOD_CK1_1 | 287 | 293 | PF00069 | 0.723 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.612 |
MOD_CK2_1 | 320 | 326 | PF00069 | 0.544 |
MOD_CK2_1 | 87 | 93 | PF00069 | 0.601 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.650 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.643 |
MOD_GlcNHglycan | 237 | 241 | PF01048 | 0.725 |
MOD_GlcNHglycan | 245 | 248 | PF01048 | 0.761 |
MOD_GSK3_1 | 267 | 274 | PF00069 | 0.622 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.728 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.688 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.648 |
MOD_N-GLC_1 | 320 | 325 | PF02516 | 0.645 |
MOD_NEK2_1 | 117 | 122 | PF00069 | 0.659 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.682 |
MOD_NEK2_1 | 284 | 289 | PF00069 | 0.722 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.660 |
MOD_NEK2_1 | 336 | 341 | PF00069 | 0.685 |
MOD_NEK2_2 | 81 | 86 | PF00069 | 0.470 |
MOD_PIKK_1 | 203 | 209 | PF00454 | 0.681 |
MOD_PK_1 | 30 | 36 | PF00069 | 0.588 |
MOD_PKA_1 | 312 | 318 | PF00069 | 0.677 |
MOD_PKA_2 | 170 | 176 | PF00069 | 0.707 |
MOD_PKA_2 | 243 | 249 | PF00069 | 0.828 |
MOD_PKA_2 | 312 | 318 | PF00069 | 0.726 |
MOD_PKA_2 | 85 | 91 | PF00069 | 0.683 |
MOD_PKA_2 | 96 | 102 | PF00069 | 0.539 |
MOD_PKB_1 | 253 | 261 | PF00069 | 0.585 |
MOD_PKB_1 | 310 | 318 | PF00069 | 0.554 |
MOD_Plk_1 | 220 | 226 | PF00069 | 0.634 |
MOD_Plk_1 | 320 | 326 | PF00069 | 0.543 |
MOD_Plk_2-3 | 320 | 326 | PF00069 | 0.608 |
MOD_Plk_4 | 264 | 270 | PF00069 | 0.619 |
MOD_Plk_4 | 336 | 342 | PF00069 | 0.697 |
TRG_DiLeu_BaEn_4 | 71 | 77 | PF01217 | 0.582 |
TRG_ENDOCYTIC_2 | 16 | 19 | PF00928 | 0.584 |
TRG_ER_diArg_1 | 253 | 256 | PF00400 | 0.594 |
TRG_ER_diArg_1 | 309 | 312 | PF00400 | 0.668 |
TRG_ER_diArg_1 | 78 | 80 | PF00400 | 0.602 |
TRG_ER_diArg_1 | 97 | 100 | PF00400 | 0.424 |
TRG_Pf-PMV_PEXEL_1 | 38 | 43 | PF00026 | 0.532 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3P5 | Leptomonas seymouri | 52% | 98% |
A0A1X0NWD2 | Trypanosomatidae | 29% | 100% |
A0A422NWQ4 | Trypanosoma rangeli | 35% | 100% |
A4HDR1 | Leishmania braziliensis | 73% | 99% |
A4I107 | Leishmania infantum | 97% | 100% |
C9ZWA2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
E9AX45 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q4QAD1 | Leishmania major | 91% | 100% |
V5BJJ9 | Trypanosoma cruzi | 34% | 99% |