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: A4ICE4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 110 | 112 | PF00675 | 0.634 |
CLV_NRD_NRD_1 | 118 | 120 | PF00675 | 0.557 |
CLV_NRD_NRD_1 | 203 | 205 | PF00675 | 0.413 |
CLV_NRD_NRD_1 | 222 | 224 | PF00675 | 0.501 |
CLV_NRD_NRD_1 | 247 | 249 | PF00675 | 0.735 |
CLV_NRD_NRD_1 | 251 | 253 | PF00675 | 0.727 |
CLV_NRD_NRD_1 | 271 | 273 | PF00675 | 0.591 |
CLV_NRD_NRD_1 | 43 | 45 | PF00675 | 0.578 |
CLV_PCSK_FUR_1 | 116 | 120 | PF00082 | 0.597 |
CLV_PCSK_KEX2_1 | 116 | 118 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 203 | 205 | PF00082 | 0.413 |
CLV_PCSK_KEX2_1 | 222 | 224 | PF00082 | 0.501 |
CLV_PCSK_KEX2_1 | 247 | 249 | PF00082 | 0.701 |
CLV_PCSK_KEX2_1 | 251 | 253 | PF00082 | 0.694 |
CLV_PCSK_KEX2_1 | 273 | 275 | PF00082 | 0.620 |
CLV_PCSK_KEX2_1 | 340 | 342 | PF00082 | 0.563 |
CLV_PCSK_KEX2_1 | 43 | 45 | PF00082 | 0.578 |
CLV_PCSK_PC1ET2_1 | 222 | 224 | PF00082 | 0.536 |
CLV_PCSK_PC1ET2_1 | 273 | 275 | PF00082 | 0.684 |
CLV_PCSK_PC1ET2_1 | 340 | 342 | PF00082 | 0.694 |
CLV_PCSK_PC7_1 | 247 | 253 | PF00082 | 0.718 |
CLV_PCSK_SKI1_1 | 104 | 108 | PF00082 | 0.614 |
CLV_PCSK_SKI1_1 | 167 | 171 | PF00082 | 0.526 |
CLV_PCSK_SKI1_1 | 196 | 200 | PF00082 | 0.525 |
CLV_PCSK_SKI1_1 | 247 | 251 | PF00082 | 0.733 |
CLV_PCSK_SKI1_1 | 4 | 8 | PF00082 | 0.643 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.575 |
DOC_CYCLIN_RxL_1 | 18 | 26 | PF00134 | 0.390 |
DOC_CYCLIN_yCln2_LP_2 | 194 | 200 | PF00134 | 0.529 |
DOC_MAPK_gen_1 | 284 | 294 | PF00069 | 0.621 |
DOC_PP4_FxxP_1 | 267 | 270 | PF00568 | 0.743 |
DOC_USP7_MATH_1 | 226 | 230 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 314 | 318 | PF00917 | 0.739 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.631 |
DOC_WW_Pin1_4 | 236 | 241 | PF00397 | 0.724 |
DOC_WW_Pin1_4 | 250 | 255 | PF00397 | 0.754 |
DOC_WW_Pin1_4 | 266 | 271 | PF00397 | 0.714 |
DOC_WW_Pin1_4 | 304 | 309 | PF00397 | 0.693 |
DOC_WW_Pin1_4 | 317 | 322 | PF00397 | 0.724 |
LIG_14-3-3_CanoR_1 | 182 | 188 | PF00244 | 0.482 |
LIG_14-3-3_CanoR_1 | 234 | 240 | PF00244 | 0.640 |
LIG_14-3-3_CanoR_1 | 30 | 39 | PF00244 | 0.599 |
LIG_BRCT_BRCA1_1 | 165 | 169 | PF00533 | 0.481 |
LIG_deltaCOP1_diTrp_1 | 275 | 283 | PF00928 | 0.642 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.631 |
LIG_FHA_2 | 134 | 140 | PF00498 | 0.671 |
LIG_FHA_2 | 147 | 153 | PF00498 | 0.679 |
LIG_FHA_2 | 168 | 174 | PF00498 | 0.497 |
LIG_FHA_2 | 197 | 203 | PF00498 | 0.454 |
LIG_FHA_2 | 291 | 297 | PF00498 | 0.536 |
LIG_FHA_2 | 68 | 74 | PF00498 | 0.426 |
LIG_LIR_Apic_2 | 282 | 286 | PF02991 | 0.683 |
LIG_LIR_Apic_2 | 83 | 88 | PF02991 | 0.589 |
LIG_LIR_Gen_1 | 137 | 144 | PF02991 | 0.583 |
LIG_LIR_Gen_1 | 70 | 80 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 137 | 143 | PF02991 | 0.595 |
LIG_LIR_Nem_3 | 166 | 171 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 176 | 181 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 335 | 339 | PF02991 | 0.557 |
LIG_LIR_Nem_3 | 70 | 75 | PF02991 | 0.421 |
LIG_MAD2 | 21 | 29 | PF02301 | 0.553 |
LIG_MLH1_MIPbox_1 | 165 | 169 | PF16413 | 0.481 |
LIG_NRBOX | 299 | 305 | PF00104 | 0.644 |
LIG_PCNA_yPIPBox_3 | 297 | 309 | PF02747 | 0.652 |
LIG_Pex14_1 | 276 | 280 | PF04695 | 0.682 |
LIG_PTB_Apo_2 | 204 | 211 | PF02174 | 0.420 |
LIG_PTB_Apo_2 | 66 | 73 | PF02174 | 0.437 |
LIG_PTB_Phospho_1 | 66 | 72 | PF10480 | 0.435 |
LIG_SH2_CRK | 178 | 182 | PF00017 | 0.437 |
LIG_SH2_CRK | 339 | 343 | PF00017 | 0.697 |
LIG_SH2_CRK | 85 | 89 | PF00017 | 0.706 |
LIG_SH2_GRB2like | 336 | 339 | PF00017 | 0.550 |
LIG_SH2_NCK_1 | 72 | 76 | PF00017 | 0.531 |
LIG_SH2_NCK_1 | 85 | 89 | PF00017 | 0.712 |
LIG_SH2_SRC | 255 | 258 | PF00017 | 0.668 |
LIG_SH2_STAT3 | 288 | 291 | PF00017 | 0.634 |
LIG_SH2_STAT5 | 216 | 219 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 46 | 49 | PF00017 | 0.446 |
LIG_SH3_3 | 26 | 32 | PF00018 | 0.622 |
LIG_SH3_3 | 275 | 281 | PF00018 | 0.608 |
LIG_TRAF2_1 | 151 | 154 | PF00917 | 0.584 |
LIG_TRAF2_1 | 293 | 296 | PF00917 | 0.500 |
LIG_TYR_ITSM | 174 | 181 | PF00017 | 0.479 |
LIG_TYR_ITSM | 68 | 75 | PF00017 | 0.532 |
LIG_WRC_WIRS_1 | 168 | 173 | PF05994 | 0.433 |
MOD_CDC14_SPxK_1 | 269 | 272 | PF00782 | 0.648 |
MOD_CDK_SPK_2 | 304 | 309 | PF00069 | 0.693 |
MOD_CDK_SPxK_1 | 266 | 272 | PF00069 | 0.674 |
MOD_CDK_SPxxK_3 | 266 | 273 | PF00069 | 0.672 |
MOD_CK1_1 | 130 | 136 | PF00069 | 0.597 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.597 |
MOD_CK1_1 | 229 | 235 | PF00069 | 0.762 |
MOD_CK1_1 | 317 | 323 | PF00069 | 0.734 |
MOD_CK2_1 | 146 | 152 | PF00069 | 0.615 |
MOD_CK2_1 | 196 | 202 | PF00069 | 0.447 |
MOD_CK2_1 | 250 | 256 | PF00069 | 0.687 |
MOD_CK2_1 | 276 | 282 | PF00069 | 0.624 |
MOD_CK2_1 | 290 | 296 | PF00069 | 0.420 |
MOD_CK2_1 | 67 | 73 | PF00069 | 0.433 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.724 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.560 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.598 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.747 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.519 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.446 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.570 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.647 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.613 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.484 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.617 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.689 |
MOD_LATS_1 | 165 | 171 | PF00433 | 0.460 |
MOD_N-GLC_1 | 144 | 149 | PF02516 | 0.629 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.503 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.580 |
MOD_NEK2_1 | 23 | 28 | PF00069 | 0.477 |
MOD_NEK2_1 | 233 | 238 | PF00069 | 0.792 |
MOD_NEK2_1 | 74 | 79 | PF00069 | 0.443 |
MOD_NEK2_2 | 183 | 188 | PF00069 | 0.481 |
MOD_PKA_1 | 222 | 228 | PF00069 | 0.678 |
MOD_PKA_2 | 222 | 228 | PF00069 | 0.641 |
MOD_PKA_2 | 233 | 239 | PF00069 | 0.640 |
MOD_Plk_1 | 127 | 133 | PF00069 | 0.699 |
MOD_Plk_1 | 173 | 179 | PF00069 | 0.404 |
MOD_Plk_2-3 | 148 | 154 | PF00069 | 0.673 |
MOD_Plk_2-3 | 290 | 296 | PF00069 | 0.617 |
MOD_Plk_4 | 173 | 179 | PF00069 | 0.422 |
MOD_Plk_4 | 196 | 202 | PF00069 | 0.447 |
MOD_ProDKin_1 | 236 | 242 | PF00069 | 0.725 |
MOD_ProDKin_1 | 250 | 256 | PF00069 | 0.753 |
MOD_ProDKin_1 | 266 | 272 | PF00069 | 0.712 |
MOD_ProDKin_1 | 304 | 310 | PF00069 | 0.696 |
MOD_ProDKin_1 | 317 | 323 | PF00069 | 0.722 |
MOD_SUMO_rev_2 | 148 | 158 | PF00179 | 0.642 |
TRG_DiLeu_BaEn_4 | 295 | 301 | PF01217 | 0.603 |
TRG_ENDOCYTIC_2 | 178 | 181 | PF00928 | 0.409 |
TRG_ENDOCYTIC_2 | 339 | 342 | PF00928 | 0.554 |
TRG_ENDOCYTIC_2 | 46 | 49 | PF00928 | 0.450 |
TRG_ENDOCYTIC_2 | 72 | 75 | PF00928 | 0.414 |
TRG_ER_diArg_1 | 116 | 119 | PF00400 | 0.599 |
TRG_ER_diArg_1 | 203 | 205 | PF00400 | 0.413 |
TRG_ER_diArg_1 | 250 | 252 | PF00400 | 0.727 |
TRG_ER_diArg_1 | 271 | 274 | PF00400 | 0.693 |
TRG_ER_diArg_1 | 341 | 344 | PF00400 | 0.640 |
TRG_ER_diArg_1 | 42 | 44 | PF00400 | 0.566 |
TRG_NLS_MonoExtC_3 | 339 | 344 | PF00514 | 0.581 |
TRG_PTS1 | 343 | 346 | PF00515 | 0.714 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P554 | Leptomonas seymouri | 66% | 92% |
A0A1X0P394 | Trypanosomatidae | 39% | 87% |
A0A3Q8IRL6 | Leishmania donovani | 100% | 100% |
A0A3R7NA51 | Trypanosoma rangeli | 49% | 97% |
A4HQ14 | Leishmania braziliensis | 81% | 100% |
D0A8V6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% |
E9ATT1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 99% |
Q4Q0R5 | Leishmania major | 90% | 98% |
V5BDN3 | Trypanosoma cruzi | 48% | 100% |