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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: A0A3S7WSS6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 123 | 125 | PF00675 | 0.721 |
CLV_NRD_NRD_1 | 142 | 144 | PF00675 | 0.492 |
CLV_NRD_NRD_1 | 163 | 165 | PF00675 | 0.803 |
CLV_NRD_NRD_1 | 196 | 198 | PF00675 | 0.651 |
CLV_NRD_NRD_1 | 206 | 208 | PF00675 | 0.562 |
CLV_NRD_NRD_1 | 254 | 256 | PF00675 | 0.738 |
CLV_NRD_NRD_1 | 346 | 348 | PF00675 | 0.674 |
CLV_PCSK_FUR_1 | 252 | 256 | PF00082 | 0.637 |
CLV_PCSK_KEX2_1 | 162 | 164 | PF00082 | 0.780 |
CLV_PCSK_KEX2_1 | 196 | 198 | PF00082 | 0.651 |
CLV_PCSK_KEX2_1 | 206 | 208 | PF00082 | 0.562 |
CLV_PCSK_KEX2_1 | 254 | 256 | PF00082 | 0.735 |
CLV_PCSK_KEX2_1 | 346 | 348 | PF00082 | 0.674 |
CLV_PCSK_PC1ET2_1 | 206 | 208 | PF00082 | 0.604 |
CLV_PCSK_SKI1_1 | 40 | 44 | PF00082 | 0.587 |
CLV_Separin_Metazoa | 116 | 120 | PF03568 | 0.509 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.488 |
DOC_CYCLIN_yCln2_LP_2 | 61 | 67 | PF00134 | 0.598 |
DOC_MAPK_gen_1 | 162 | 172 | PF00069 | 0.727 |
DOC_MAPK_gen_1 | 196 | 202 | PF00069 | 0.650 |
DOC_MAPK_gen_1 | 34 | 43 | PF00069 | 0.514 |
DOC_MAPK_MEF2A_6 | 163 | 172 | PF00069 | 0.725 |
DOC_PP2B_LxvP_1 | 65 | 68 | PF13499 | 0.556 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.813 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.510 |
DOC_USP7_MATH_1 | 178 | 182 | PF00917 | 0.686 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 225 | 229 | PF00917 | 0.747 |
DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.720 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.734 |
DOC_USP7_MATH_1 | 294 | 298 | PF00917 | 0.726 |
DOC_USP7_MATH_1 | 311 | 315 | PF00917 | 0.810 |
DOC_USP7_MATH_1 | 96 | 100 | PF00917 | 0.565 |
DOC_USP7_UBL2_3 | 144 | 148 | PF12436 | 0.736 |
DOC_WW_Pin1_4 | 275 | 280 | PF00397 | 0.706 |
DOC_WW_Pin1_4 | 299 | 304 | PF00397 | 0.807 |
DOC_WW_Pin1_4 | 327 | 332 | PF00397 | 0.792 |
LIG_14-3-3_CanoR_1 | 106 | 110 | PF00244 | 0.587 |
LIG_14-3-3_CanoR_1 | 197 | 203 | PF00244 | 0.646 |
LIG_14-3-3_CanoR_1 | 222 | 230 | PF00244 | 0.794 |
LIG_14-3-3_CanoR_1 | 258 | 266 | PF00244 | 0.830 |
LIG_14-3-3_CanoR_1 | 269 | 274 | PF00244 | 0.767 |
LIG_14-3-3_CanoR_1 | 275 | 279 | PF00244 | 0.555 |
LIG_14-3-3_CanoR_1 | 360 | 370 | PF00244 | 0.635 |
LIG_Actin_WH2_2 | 103 | 121 | PF00022 | 0.566 |
LIG_BIR_III_2 | 291 | 295 | PF00653 | 0.598 |
LIG_FHA_1 | 221 | 227 | PF00498 | 0.711 |
LIG_FHA_1 | 241 | 247 | PF00498 | 0.728 |
LIG_FHA_1 | 268 | 274 | PF00498 | 0.735 |
LIG_FHA_1 | 279 | 285 | PF00498 | 0.536 |
LIG_FHA_1 | 310 | 316 | PF00498 | 0.765 |
LIG_FHA_1 | 333 | 339 | PF00498 | 0.727 |
LIG_FHA_1 | 363 | 369 | PF00498 | 0.645 |
LIG_FHA_2 | 305 | 311 | PF00498 | 0.699 |
LIG_Integrin_isoDGR_2 | 141 | 143 | PF01839 | 0.730 |
LIG_LIR_Gen_1 | 102 | 110 | PF02991 | 0.339 |
LIG_LIR_Gen_1 | 18 | 29 | PF02991 | 0.513 |
LIG_LIR_Gen_1 | 212 | 219 | PF02991 | 0.653 |
LIG_LIR_Gen_1 | 287 | 296 | PF02991 | 0.674 |
LIG_LIR_Gen_1 | 30 | 38 | PF02991 | 0.252 |
LIG_LIR_Gen_1 | 82 | 90 | PF02991 | 0.586 |
LIG_LIR_Nem_3 | 102 | 107 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 18 | 24 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 212 | 217 | PF02991 | 0.625 |
LIG_LIR_Nem_3 | 371 | 377 | PF02991 | 0.611 |
LIG_LIR_Nem_3 | 82 | 86 | PF02991 | 0.590 |
LIG_SH2_STAP1 | 32 | 36 | PF00017 | 0.514 |
LIG_SH3_1 | 162 | 168 | PF00018 | 0.731 |
LIG_SH3_3 | 151 | 157 | PF00018 | 0.762 |
LIG_SH3_3 | 162 | 168 | PF00018 | 0.592 |
LIG_SH3_3 | 297 | 303 | PF00018 | 0.660 |
LIG_SH3_3 | 328 | 334 | PF00018 | 0.788 |
LIG_SH3_3 | 45 | 51 | PF00018 | 0.535 |
LIG_SH3_3 | 61 | 67 | PF00018 | 0.368 |
LIG_SH3_4 | 146 | 153 | PF00018 | 0.736 |
LIG_TRAF2_1 | 265 | 268 | PF00917 | 0.733 |
MOD_CK1_1 | 181 | 187 | PF00069 | 0.699 |
MOD_CK1_1 | 190 | 196 | PF00069 | 0.640 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.686 |
MOD_CK1_1 | 261 | 267 | PF00069 | 0.721 |
MOD_CK1_1 | 278 | 284 | PF00069 | 0.633 |
MOD_CK1_1 | 304 | 310 | PF00069 | 0.803 |
MOD_CK1_1 | 314 | 320 | PF00069 | 0.793 |
MOD_CK1_1 | 332 | 338 | PF00069 | 0.674 |
MOD_CK1_1 | 339 | 345 | PF00069 | 0.523 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.540 |
MOD_CK2_1 | 230 | 236 | PF00069 | 0.685 |
MOD_CK2_1 | 245 | 251 | PF00069 | 0.748 |
MOD_CK2_1 | 96 | 102 | PF00069 | 0.647 |
MOD_Cter_Amidation | 141 | 144 | PF01082 | 0.727 |
MOD_DYRK1A_RPxSP_1 | 275 | 279 | PF00069 | 0.728 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.790 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.580 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.776 |
MOD_GlcNHglycan | 317 | 320 | PF01048 | 0.785 |
MOD_GlcNHglycan | 324 | 328 | PF01048 | 0.796 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.601 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.646 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.635 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.452 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.669 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.635 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.712 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.673 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.798 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.785 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.662 |
MOD_N-GLC_1 | 15 | 20 | PF02516 | 0.497 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.598 |
MOD_NEK2_1 | 149 | 154 | PF00069 | 0.721 |
MOD_NEK2_1 | 195 | 200 | PF00069 | 0.664 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.639 |
MOD_NEK2_1 | 240 | 245 | PF00069 | 0.674 |
MOD_NEK2_1 | 284 | 289 | PF00069 | 0.781 |
MOD_NEK2_1 | 361 | 366 | PF00069 | 0.705 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.509 |
MOD_NEK2_2 | 311 | 316 | PF00069 | 0.811 |
MOD_PIKK_1 | 190 | 196 | PF00454 | 0.684 |
MOD_PIKK_1 | 217 | 223 | PF00454 | 0.691 |
MOD_PIKK_1 | 258 | 264 | PF00454 | 0.731 |
MOD_PKA_2 | 105 | 111 | PF00069 | 0.594 |
MOD_PKA_2 | 195 | 201 | PF00069 | 0.666 |
MOD_PKA_2 | 221 | 227 | PF00069 | 0.750 |
MOD_PKA_2 | 274 | 280 | PF00069 | 0.645 |
MOD_PKA_2 | 30 | 36 | PF00069 | 0.526 |
MOD_PKA_2 | 72 | 78 | PF00069 | 0.595 |
MOD_PKB_1 | 258 | 266 | PF00069 | 0.745 |
MOD_Plk_1 | 15 | 21 | PF00069 | 0.495 |
MOD_Plk_1 | 323 | 329 | PF00069 | 0.785 |
MOD_Plk_1 | 370 | 376 | PF00069 | 0.565 |
MOD_Plk_4 | 105 | 111 | PF00069 | 0.548 |
MOD_Plk_4 | 16 | 22 | PF00069 | 0.399 |
MOD_Plk_4 | 285 | 291 | PF00069 | 0.784 |
MOD_Plk_4 | 4 | 10 | PF00069 | 0.486 |
MOD_ProDKin_1 | 275 | 281 | PF00069 | 0.705 |
MOD_ProDKin_1 | 299 | 305 | PF00069 | 0.807 |
MOD_ProDKin_1 | 327 | 333 | PF00069 | 0.790 |
TRG_DiLeu_BaLyEn_6 | 280 | 285 | PF01217 | 0.703 |
TRG_ENDOCYTIC_2 | 21 | 24 | PF00928 | 0.444 |
TRG_ENDOCYTIC_2 | 290 | 293 | PF00928 | 0.776 |
TRG_ENDOCYTIC_2 | 32 | 35 | PF00928 | 0.294 |
TRG_ER_diArg_1 | 162 | 164 | PF00400 | 0.825 |
TRG_ER_diArg_1 | 195 | 197 | PF00400 | 0.653 |
TRG_ER_diArg_1 | 252 | 255 | PF00400 | 0.754 |
TRG_ER_diArg_1 | 345 | 347 | PF00400 | 0.676 |
TRG_ER_diArg_1 | 354 | 357 | PF00400 | 0.525 |
TRG_NLS_MonoExtC_3 | 142 | 147 | PF00514 | 0.640 |
TRG_Pf-PMV_PEXEL_1 | 347 | 351 | PF00026 | 0.632 |
TRG_Pf-PMV_PEXEL_1 | 55 | 59 | PF00026 | 0.544 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PB18 | Leptomonas seymouri | 51% | 97% |
A4H7H0 | Leishmania braziliensis | 72% | 99% |
A4HVV1 | Leishmania infantum | 99% | 100% |
C9ZT76 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 84% |
E9APK3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4QFX6 | Leishmania major | 94% | 100% |