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: Q4Q390
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 242 | 246 | PF00656 | 0.612 |
CLV_NRD_NRD_1 | 382 | 384 | PF00675 | 0.467 |
CLV_PCSK_KEX2_1 | 381 | 383 | PF00082 | 0.458 |
CLV_PCSK_PC1ET2_1 | 381 | 383 | PF00082 | 0.460 |
CLV_PCSK_SKI1_1 | 192 | 196 | PF00082 | 0.611 |
CLV_PCSK_SKI1_1 | 201 | 205 | PF00082 | 0.556 |
CLV_PCSK_SKI1_1 | 265 | 269 | PF00082 | 0.733 |
CLV_PCSK_SKI1_1 | 30 | 34 | PF00082 | 0.692 |
CLV_PCSK_SKI1_1 | 53 | 57 | PF00082 | 0.517 |
DEG_APCC_DBOX_1 | 191 | 199 | PF00400 | 0.608 |
DEG_SPOP_SBC_1 | 126 | 130 | PF00917 | 0.553 |
DOC_CYCLIN_RxL_1 | 189 | 199 | PF00134 | 0.609 |
DOC_MAPK_HePTP_8 | 90 | 102 | PF00069 | 0.553 |
DOC_MAPK_MEF2A_6 | 251 | 260 | PF00069 | 0.557 |
DOC_MAPK_MEF2A_6 | 84 | 92 | PF00069 | 0.533 |
DOC_MAPK_MEF2A_6 | 93 | 102 | PF00069 | 0.536 |
DOC_PP2B_PxIxI_1 | 97 | 103 | PF00149 | 0.554 |
DOC_PP4_FxxP_1 | 74 | 77 | PF00568 | 0.604 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.490 |
DOC_USP7_MATH_1 | 176 | 180 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 306 | 310 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 48 | 52 | PF00917 | 0.768 |
DOC_WW_Pin1_4 | 203 | 208 | PF00397 | 0.598 |
DOC_WW_Pin1_4 | 209 | 214 | PF00397 | 0.588 |
DOC_WW_Pin1_4 | 219 | 224 | PF00397 | 0.573 |
DOC_WW_Pin1_4 | 44 | 49 | PF00397 | 0.641 |
LIG_14-3-3_CanoR_1 | 124 | 133 | PF00244 | 0.532 |
LIG_14-3-3_CanoR_1 | 174 | 184 | PF00244 | 0.610 |
LIG_14-3-3_CanoR_1 | 295 | 302 | PF00244 | 0.601 |
LIG_14-3-3_CanoR_1 | 53 | 58 | PF00244 | 0.521 |
LIG_14-3-3_CanoR_1 | 7 | 13 | PF00244 | 0.593 |
LIG_14-3-3_CterR_2 | 382 | 385 | PF00244 | 0.628 |
LIG_Actin_WH2_2 | 187 | 203 | PF00022 | 0.642 |
LIG_Actin_WH2_2 | 340 | 355 | PF00022 | 0.483 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.619 |
LIG_BIR_III_2 | 45 | 49 | PF00653 | 0.596 |
LIG_BRCT_BRCA1_1 | 129 | 133 | PF00533 | 0.547 |
LIG_deltaCOP1_diTrp_1 | 280 | 283 | PF00928 | 0.477 |
LIG_FHA_1 | 147 | 153 | PF00498 | 0.545 |
LIG_FHA_1 | 179 | 185 | PF00498 | 0.652 |
LIG_FHA_1 | 77 | 83 | PF00498 | 0.607 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.554 |
LIG_FHA_2 | 286 | 292 | PF00498 | 0.524 |
LIG_FHA_2 | 357 | 363 | PF00498 | 0.577 |
LIG_FHA_2 | 366 | 372 | PF00498 | 0.576 |
LIG_FHA_2 | 54 | 60 | PF00498 | 0.486 |
LIG_FHA_2 | 89 | 95 | PF00498 | 0.560 |
LIG_LIR_Apic_2 | 280 | 284 | PF02991 | 0.483 |
LIG_LIR_Apic_2 | 71 | 77 | PF02991 | 0.597 |
LIG_LIR_Gen_1 | 101 | 111 | PF02991 | 0.573 |
LIG_LIR_Gen_1 | 362 | 372 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 101 | 107 | PF02991 | 0.584 |
LIG_LIR_Nem_3 | 2 | 8 | PF02991 | 0.628 |
LIG_LIR_Nem_3 | 280 | 286 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 362 | 367 | PF02991 | 0.563 |
LIG_SH2_CRK | 104 | 108 | PF00017 | 0.543 |
LIG_SH3_2 | 210 | 215 | PF14604 | 0.583 |
LIG_SH3_3 | 204 | 210 | PF00018 | 0.585 |
LIG_SH3_3 | 217 | 223 | PF00018 | 0.616 |
LIG_SH3_3 | 335 | 341 | PF00018 | 0.574 |
LIG_SUMO_SIM_anti_2 | 334 | 340 | PF11976 | 0.581 |
LIG_SUMO_SIM_par_1 | 146 | 154 | PF11976 | 0.580 |
LIG_TYR_ITIM | 102 | 107 | PF00017 | 0.526 |
LIG_WRC_WIRS_1 | 1 | 6 | PF05994 | 0.559 |
LIG_WRC_WIRS_1 | 361 | 366 | PF05994 | 0.566 |
MOD_CDC14_SPxK_1 | 212 | 215 | PF00782 | 0.587 |
MOD_CDK_SPxK_1 | 209 | 215 | PF00069 | 0.582 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.601 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.715 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.598 |
MOD_CK1_1 | 222 | 228 | PF00069 | 0.581 |
MOD_CK1_1 | 301 | 307 | PF00069 | 0.588 |
MOD_CK1_1 | 355 | 361 | PF00069 | 0.537 |
MOD_CK1_1 | 47 | 53 | PF00069 | 0.588 |
MOD_CK2_1 | 113 | 119 | PF00069 | 0.541 |
MOD_CK2_1 | 163 | 169 | PF00069 | 0.621 |
MOD_CK2_1 | 285 | 291 | PF00069 | 0.511 |
MOD_CK2_1 | 356 | 362 | PF00069 | 0.550 |
MOD_CK2_1 | 365 | 371 | PF00069 | 0.535 |
MOD_CK2_1 | 53 | 59 | PF00069 | 0.504 |
MOD_CK2_1 | 88 | 94 | PF00069 | 0.544 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.754 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.707 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.655 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.501 |
MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.600 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.517 |
MOD_GlcNHglycan | 49 | 53 | PF01048 | 0.670 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.578 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.535 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.632 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.621 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.668 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.559 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.514 |
MOD_GSK3_1 | 351 | 358 | PF00069 | 0.504 |
MOD_GSK3_1 | 362 | 369 | PF00069 | 0.549 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.627 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.555 |
MOD_N-GLC_1 | 19 | 24 | PF02516 | 0.657 |
MOD_NEK2_1 | 127 | 132 | PF00069 | 0.595 |
MOD_NEK2_1 | 151 | 156 | PF00069 | 0.609 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.583 |
MOD_NEK2_1 | 256 | 261 | PF00069 | 0.459 |
MOD_NEK2_1 | 352 | 357 | PF00069 | 0.570 |
MOD_PIKK_1 | 132 | 138 | PF00454 | 0.536 |
MOD_PIKK_1 | 15 | 21 | PF00454 | 0.592 |
MOD_PIKK_1 | 184 | 190 | PF00454 | 0.595 |
MOD_PIKK_1 | 295 | 301 | PF00454 | 0.661 |
MOD_PIKK_1 | 339 | 345 | PF00454 | 0.395 |
MOD_PIKK_1 | 76 | 82 | PF00454 | 0.592 |
MOD_PKA_2 | 176 | 182 | PF00069 | 0.621 |
MOD_PKA_2 | 286 | 292 | PF00069 | 0.509 |
MOD_PKA_2 | 92 | 98 | PF00069 | 0.532 |
MOD_PKB_1 | 295 | 303 | PF00069 | 0.536 |
MOD_Plk_1 | 25 | 31 | PF00069 | 0.626 |
MOD_Plk_1 | 265 | 271 | PF00069 | 0.654 |
MOD_Plk_1 | 333 | 339 | PF00069 | 0.592 |
MOD_Plk_4 | 146 | 152 | PF00069 | 0.583 |
MOD_Plk_4 | 333 | 339 | PF00069 | 0.592 |
MOD_ProDKin_1 | 203 | 209 | PF00069 | 0.600 |
MOD_ProDKin_1 | 219 | 225 | PF00069 | 0.573 |
MOD_ProDKin_1 | 44 | 50 | PF00069 | 0.640 |
TRG_DiLeu_BaEn_1 | 110 | 115 | PF01217 | 0.544 |
TRG_DiLeu_BaLyEn_6 | 258 | 263 | PF01217 | 0.513 |
TRG_ENDOCYTIC_2 | 104 | 107 | PF00928 | 0.557 |
TRG_ER_diArg_1 | 294 | 297 | PF00400 | 0.592 |
TRG_ER_diArg_1 | 382 | 384 | PF00400 | 0.468 |
TRG_NES_CRM1_1 | 80 | 94 | PF08389 | 0.529 |
TRG_Pf-PMV_PEXEL_1 | 192 | 196 | PF00026 | 0.611 |
TRG_Pf-PMV_PEXEL_1 | 261 | 266 | PF00026 | 0.594 |
TRG_Pf-PMV_PEXEL_1 | 276 | 280 | PF00026 | 0.407 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HWJ1 | Leptomonas seymouri | 52% | 79% |
A0A3Q8IH36 | Leishmania donovani | 95% | 100% |
A4HAN3 | Leishmania braziliensis | 78% | 100% |
A4I9S5 | Leishmania infantum | 95% | 100% |
E9B4T6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |