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: Q4QDN4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 110 | 114 | PF00656 | 0.527 |
CLV_NRD_NRD_1 | 175 | 177 | PF00675 | 0.529 |
CLV_NRD_NRD_1 | 201 | 203 | PF00675 | 0.570 |
CLV_NRD_NRD_1 | 204 | 206 | PF00675 | 0.540 |
CLV_NRD_NRD_1 | 247 | 249 | PF00675 | 0.658 |
CLV_NRD_NRD_1 | 388 | 390 | PF00675 | 0.655 |
CLV_PCSK_FUR_1 | 202 | 206 | PF00082 | 0.546 |
CLV_PCSK_KEX2_1 | 175 | 177 | PF00082 | 0.529 |
CLV_PCSK_KEX2_1 | 201 | 203 | PF00082 | 0.570 |
CLV_PCSK_KEX2_1 | 204 | 206 | PF00082 | 0.540 |
CLV_PCSK_KEX2_1 | 247 | 249 | PF00082 | 0.658 |
CLV_PCSK_KEX2_1 | 40 | 42 | PF00082 | 0.608 |
CLV_PCSK_PC1ET2_1 | 40 | 42 | PF00082 | 0.608 |
CLV_PCSK_PC7_1 | 197 | 203 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 165 | 169 | PF00082 | 0.590 |
CLV_PCSK_SKI1_1 | 247 | 251 | PF00082 | 0.795 |
CLV_PCSK_SKI1_1 | 376 | 380 | PF00082 | 0.654 |
CLV_PCSK_SKI1_1 | 40 | 44 | PF00082 | 0.522 |
CLV_PCSK_SKI1_1 | 77 | 81 | PF00082 | 0.530 |
DEG_SPOP_SBC_1 | 361 | 365 | PF00917 | 0.630 |
DOC_CDC14_PxL_1 | 207 | 215 | PF14671 | 0.622 |
DOC_MAPK_gen_1 | 175 | 182 | PF00069 | 0.461 |
DOC_MAPK_MEF2A_6 | 175 | 184 | PF00069 | 0.452 |
DOC_MAPK_MEF2A_6 | 329 | 338 | PF00069 | 0.413 |
DOC_PP1_RVXF_1 | 33 | 39 | PF00149 | 0.486 |
DOC_PP2B_LxvP_1 | 251 | 254 | PF13499 | 0.558 |
DOC_PP4_FxxP_1 | 250 | 253 | PF00568 | 0.560 |
DOC_USP7_MATH_1 | 218 | 222 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 225 | 229 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 260 | 264 | PF00917 | 0.737 |
DOC_USP7_MATH_1 | 360 | 364 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.740 |
DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.598 |
DOC_WW_Pin1_4 | 223 | 228 | PF00397 | 0.508 |
DOC_WW_Pin1_4 | 239 | 244 | PF00397 | 0.739 |
DOC_WW_Pin1_4 | 249 | 254 | PF00397 | 0.635 |
LIG_14-3-3_CanoR_1 | 122 | 128 | PF00244 | 0.375 |
LIG_14-3-3_CanoR_1 | 165 | 171 | PF00244 | 0.508 |
LIG_14-3-3_CanoR_1 | 283 | 290 | PF00244 | 0.574 |
LIG_14-3-3_CanoR_1 | 295 | 300 | PF00244 | 0.602 |
LIG_Actin_WH2_2 | 400 | 417 | PF00022 | 0.569 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.811 |
LIG_BIR_III_1 | 1 | 5 | PF00653 | 0.733 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.733 |
LIG_Clathr_ClatBox_1 | 396 | 400 | PF01394 | 0.539 |
LIG_FHA_1 | 166 | 172 | PF00498 | 0.452 |
LIG_FHA_1 | 283 | 289 | PF00498 | 0.579 |
LIG_FHA_1 | 70 | 76 | PF00498 | 0.574 |
LIG_FHA_2 | 153 | 159 | PF00498 | 0.432 |
LIG_FHA_2 | 369 | 375 | PF00498 | 0.683 |
LIG_LIR_Gen_1 | 155 | 164 | PF02991 | 0.576 |
LIG_LIR_Nem_3 | 155 | 160 | PF02991 | 0.570 |
LIG_LIR_Nem_3 | 200 | 206 | PF02991 | 0.553 |
LIG_LIR_Nem_3 | 208 | 213 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 99 | 105 | PF02991 | 0.489 |
LIG_LYPXL_yS_3 | 210 | 213 | PF13949 | 0.603 |
LIG_NRBOX | 179 | 185 | PF00104 | 0.555 |
LIG_PDZ_Class_2 | 414 | 419 | PF00595 | 0.686 |
LIG_Pex14_1 | 203 | 207 | PF04695 | 0.635 |
LIG_Pex14_2 | 50 | 54 | PF04695 | 0.507 |
LIG_REV1ctd_RIR_1 | 47 | 55 | PF16727 | 0.511 |
LIG_SH2_CRK | 157 | 161 | PF00017 | 0.584 |
LIG_SH2_CRK | 188 | 192 | PF00017 | 0.458 |
LIG_SH2_STAP1 | 128 | 132 | PF00017 | 0.444 |
LIG_SH2_STAP1 | 166 | 170 | PF00017 | 0.498 |
LIG_SH2_STAT3 | 377 | 380 | PF00017 | 0.632 |
LIG_SH2_STAT5 | 330 | 333 | PF00017 | 0.532 |
LIG_SH2_STAT5 | 337 | 340 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 37 | 40 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 53 | 56 | PF00017 | 0.519 |
LIG_SH3_3 | 251 | 257 | PF00018 | 0.591 |
LIG_SUMO_SIM_par_1 | 394 | 400 | PF11976 | 0.489 |
MOD_CDC14_SPxK_1 | 244 | 247 | PF00782 | 0.720 |
MOD_CDC14_SPxK_1 | 252 | 255 | PF00782 | 0.659 |
MOD_CDK_SPxK_1 | 241 | 247 | PF00069 | 0.720 |
MOD_CDK_SPxK_1 | 249 | 255 | PF00069 | 0.662 |
MOD_CDK_SPxxK_3 | 241 | 248 | PF00069 | 0.784 |
MOD_CK1_1 | 221 | 227 | PF00069 | 0.606 |
MOD_CK1_1 | 262 | 268 | PF00069 | 0.695 |
MOD_CK1_1 | 364 | 370 | PF00069 | 0.560 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.606 |
MOD_CK2_1 | 368 | 374 | PF00069 | 0.653 |
MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.511 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.633 |
MOD_GlcNHglycan | 194 | 197 | PF01048 | 0.608 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.648 |
MOD_GlcNHglycan | 227 | 230 | PF01048 | 0.615 |
MOD_GlcNHglycan | 232 | 236 | PF01048 | 0.524 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.746 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.672 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.652 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.704 |
MOD_GlcNHglycan | 382 | 385 | PF01048 | 0.535 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.767 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.675 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.292 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.503 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.643 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.745 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.531 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.563 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.644 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.767 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.520 |
MOD_LATS_1 | 139 | 145 | PF00433 | 0.553 |
MOD_LATS_1 | 78 | 84 | PF00433 | 0.570 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.394 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.645 |
MOD_NEK2_1 | 306 | 311 | PF00069 | 0.654 |
MOD_NEK2_1 | 313 | 318 | PF00069 | 0.562 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.503 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.486 |
MOD_NEK2_2 | 123 | 128 | PF00069 | 0.543 |
MOD_NEK2_2 | 368 | 373 | PF00069 | 0.557 |
MOD_PKA_2 | 282 | 288 | PF00069 | 0.657 |
MOD_PKA_2 | 306 | 312 | PF00069 | 0.626 |
MOD_PKA_2 | 380 | 386 | PF00069 | 0.639 |
MOD_PKB_1 | 295 | 303 | PF00069 | 0.652 |
MOD_Plk_1 | 301 | 307 | PF00069 | 0.536 |
MOD_Plk_1 | 4 | 10 | PF00069 | 0.793 |
MOD_Plk_4 | 123 | 129 | PF00069 | 0.443 |
MOD_Plk_4 | 152 | 158 | PF00069 | 0.418 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.570 |
MOD_Plk_4 | 262 | 268 | PF00069 | 0.676 |
MOD_Plk_4 | 70 | 76 | PF00069 | 0.571 |
MOD_ProDKin_1 | 223 | 229 | PF00069 | 0.515 |
MOD_ProDKin_1 | 239 | 245 | PF00069 | 0.739 |
MOD_ProDKin_1 | 249 | 255 | PF00069 | 0.635 |
MOD_SUMO_for_1 | 132 | 135 | PF00179 | 0.483 |
MOD_SUMO_rev_2 | 383 | 392 | PF00179 | 0.652 |
TRG_ENDOCYTIC_2 | 157 | 160 | PF00928 | 0.573 |
TRG_ENDOCYTIC_2 | 188 | 191 | PF00928 | 0.535 |
TRG_ENDOCYTIC_2 | 210 | 213 | PF00928 | 0.603 |
TRG_ER_diArg_1 | 174 | 176 | PF00400 | 0.376 |
TRG_ER_diArg_1 | 201 | 203 | PF00400 | 0.570 |
TRG_ER_diArg_1 | 204 | 206 | PF00400 | 0.540 |
TRG_ER_diArg_1 | 246 | 248 | PF00400 | 0.676 |
TRG_ER_diArg_1 | 294 | 297 | PF00400 | 0.557 |
TRG_Pf-PMV_PEXEL_1 | 204 | 208 | PF00026 | 0.513 |
TRG_Pf-PMV_PEXEL_1 | 329 | 333 | PF00026 | 0.415 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZP2 | Leptomonas seymouri | 45% | 99% |
A0A3S7WV66 | Leishmania donovani | 91% | 100% |
A4H9Q7 | Leishmania braziliensis | 70% | 100% |
A4HY26 | Leishmania infantum | 92% | 100% |
E9ART9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 99% |