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: Q4Q106
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 420 | 424 | PF00656 | 0.618 |
CLV_C14_Caspase3-7 | 56 | 60 | PF00656 | 0.651 |
CLV_NRD_NRD_1 | 133 | 135 | PF00675 | 0.514 |
CLV_NRD_NRD_1 | 237 | 239 | PF00675 | 0.663 |
CLV_NRD_NRD_1 | 396 | 398 | PF00675 | 0.522 |
CLV_NRD_NRD_1 | 85 | 87 | PF00675 | 0.449 |
CLV_PCSK_FUR_1 | 278 | 282 | PF00082 | 0.639 |
CLV_PCSK_KEX2_1 | 133 | 135 | PF00082 | 0.490 |
CLV_PCSK_KEX2_1 | 280 | 282 | PF00082 | 0.686 |
CLV_PCSK_KEX2_1 | 352 | 354 | PF00082 | 0.515 |
CLV_PCSK_KEX2_1 | 396 | 398 | PF00082 | 0.513 |
CLV_PCSK_KEX2_1 | 85 | 87 | PF00082 | 0.449 |
CLV_PCSK_PC1ET2_1 | 280 | 282 | PF00082 | 0.683 |
CLV_PCSK_PC1ET2_1 | 352 | 354 | PF00082 | 0.515 |
CLV_PCSK_SKI1_1 | 113 | 117 | PF00082 | 0.403 |
CLV_PCSK_SKI1_1 | 255 | 259 | PF00082 | 0.637 |
CLV_PCSK_SKI1_1 | 29 | 33 | PF00082 | 0.556 |
CLV_PCSK_SKI1_1 | 316 | 320 | PF00082 | 0.520 |
CLV_PCSK_SKI1_1 | 352 | 356 | PF00082 | 0.512 |
CLV_PCSK_SKI1_1 | 419 | 423 | PF00082 | 0.502 |
DEG_APCC_DBOX_1 | 315 | 323 | PF00400 | 0.518 |
DEG_MDM2_SWIB_1 | 158 | 165 | PF02201 | 0.382 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.654 |
DEG_SPOP_SBC_1 | 191 | 195 | PF00917 | 0.642 |
DEG_SPOP_SBC_1 | 51 | 55 | PF00917 | 0.715 |
DOC_CYCLIN_RxL_1 | 252 | 261 | PF00134 | 0.614 |
DOC_CYCLIN_RxL_1 | 349 | 359 | PF00134 | 0.516 |
DOC_CYCLIN_yCln2_LP_2 | 135 | 141 | PF00134 | 0.507 |
DOC_CYCLIN_yCln2_LP_2 | 31 | 34 | PF00134 | 0.608 |
DOC_MAPK_DCC_7 | 293 | 303 | PF00069 | 0.605 |
DOC_MAPK_DCC_7 | 316 | 324 | PF00069 | 0.510 |
DOC_MAPK_MEF2A_6 | 316 | 324 | PF00069 | 0.510 |
DOC_PP2B_LxvP_1 | 135 | 138 | PF13499 | 0.432 |
DOC_PP2B_LxvP_1 | 265 | 268 | PF13499 | 0.678 |
DOC_PP2B_LxvP_1 | 31 | 34 | PF13499 | 0.681 |
DOC_PP4_FxxP_1 | 65 | 68 | PF00568 | 0.469 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.459 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.306 |
DOC_USP7_MATH_1 | 288 | 292 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 341 | 345 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 356 | 360 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 364 | 368 | PF00917 | 0.515 |
DOC_USP7_MATH_1 | 51 | 55 | PF00917 | 0.701 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.504 |
DOC_WW_Pin1_4 | 205 | 210 | PF00397 | 0.697 |
DOC_WW_Pin1_4 | 258 | 263 | PF00397 | 0.601 |
DOC_WW_Pin1_4 | 32 | 37 | PF00397 | 0.575 |
LIG_14-3-3_CanoR_1 | 113 | 122 | PF00244 | 0.472 |
LIG_14-3-3_CanoR_1 | 188 | 198 | PF00244 | 0.556 |
LIG_14-3-3_CanoR_1 | 202 | 209 | PF00244 | 0.605 |
LIG_14-3-3_CanoR_1 | 255 | 261 | PF00244 | 0.612 |
LIG_14-3-3_CanoR_1 | 373 | 378 | PF00244 | 0.545 |
LIG_14-3-3_CanoR_1 | 86 | 92 | PF00244 | 0.422 |
LIG_BRCT_BRCA1_1 | 154 | 158 | PF00533 | 0.382 |
LIG_BRCT_BRCA1_1 | 290 | 294 | PF00533 | 0.548 |
LIG_DLG_GKlike_1 | 373 | 381 | PF00625 | 0.436 |
LIG_eIF4E_1 | 9 | 15 | PF01652 | 0.580 |
LIG_EVH1_2 | 68 | 72 | PF00568 | 0.580 |
LIG_FHA_1 | 10 | 16 | PF00498 | 0.573 |
LIG_FHA_1 | 114 | 120 | PF00498 | 0.418 |
LIG_FHA_1 | 17 | 23 | PF00498 | 0.513 |
LIG_FHA_1 | 298 | 304 | PF00498 | 0.592 |
LIG_FHA_1 | 372 | 378 | PF00498 | 0.514 |
LIG_FHA_2 | 35 | 41 | PF00498 | 0.499 |
LIG_FHA_2 | 54 | 60 | PF00498 | 0.505 |
LIG_LIR_Gen_1 | 155 | 166 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 155 | 161 | PF02991 | 0.383 |
LIG_NRBOX | 40 | 46 | PF00104 | 0.557 |
LIG_PCNA_yPIPBox_3 | 408 | 422 | PF02747 | 0.506 |
LIG_Pex14_2 | 127 | 131 | PF04695 | 0.402 |
LIG_Pex14_2 | 154 | 158 | PF04695 | 0.411 |
LIG_SH2_STAP1 | 350 | 354 | PF00017 | 0.516 |
LIG_SH2_STAT3 | 149 | 152 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 160 | 163 | PF00017 | 0.368 |
LIG_SH2_STAT5 | 276 | 279 | PF00017 | 0.629 |
LIG_SH2_STAT5 | 410 | 413 | PF00017 | 0.468 |
LIG_SH3_3 | 116 | 122 | PF00018 | 0.507 |
LIG_SH3_3 | 30 | 36 | PF00018 | 0.522 |
LIG_SH3_3 | 314 | 320 | PF00018 | 0.661 |
LIG_SH3_3 | 333 | 339 | PF00018 | 0.507 |
LIG_SUMO_SIM_anti_2 | 300 | 305 | PF11976 | 0.597 |
LIG_SUMO_SIM_par_1 | 256 | 261 | PF11976 | 0.612 |
LIG_SUMO_SIM_par_1 | 373 | 378 | PF11976 | 0.590 |
MOD_CDK_SPK_2 | 2 | 7 | PF00069 | 0.504 |
MOD_CK1_1 | 192 | 198 | PF00069 | 0.638 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.625 |
MOD_CK1_1 | 223 | 229 | PF00069 | 0.573 |
MOD_CK1_1 | 357 | 363 | PF00069 | 0.591 |
MOD_CK1_1 | 371 | 377 | PF00069 | 0.433 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.569 |
MOD_CK2_1 | 34 | 40 | PF00069 | 0.509 |
MOD_Cter_Amidation | 278 | 281 | PF01082 | 0.688 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.769 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.650 |
MOD_GlcNHglycan | 241 | 244 | PF01048 | 0.628 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.636 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.631 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.653 |
MOD_GlcNHglycan | 342 | 346 | PF01048 | 0.571 |
MOD_GlcNHglycan | 356 | 359 | PF01048 | 0.620 |
MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.497 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.614 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.592 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.374 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.392 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.663 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.429 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.630 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.641 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.508 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.618 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.745 |
MOD_N-GLC_1 | 248 | 253 | PF02516 | 0.577 |
MOD_N-GLC_1 | 362 | 367 | PF02516 | 0.581 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.352 |
MOD_NEK2_1 | 114 | 119 | PF00069 | 0.425 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.536 |
MOD_NEK2_1 | 220 | 225 | PF00069 | 0.666 |
MOD_NEK2_1 | 233 | 238 | PF00069 | 0.538 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.558 |
MOD_NEK2_1 | 354 | 359 | PF00069 | 0.500 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.590 |
MOD_NEK2_2 | 139 | 144 | PF00069 | 0.500 |
MOD_NEK2_2 | 153 | 158 | PF00069 | 0.366 |
MOD_PKA_2 | 182 | 188 | PF00069 | 0.512 |
MOD_PKA_2 | 198 | 204 | PF00069 | 0.796 |
MOD_Plk_2-3 | 425 | 431 | PF00069 | 0.500 |
MOD_Plk_4 | 153 | 159 | PF00069 | 0.369 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.402 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.503 |
MOD_ProDKin_1 | 205 | 211 | PF00069 | 0.696 |
MOD_ProDKin_1 | 258 | 264 | PF00069 | 0.600 |
MOD_ProDKin_1 | 32 | 38 | PF00069 | 0.568 |
MOD_SUMO_rev_2 | 174 | 182 | PF00179 | 0.593 |
TRG_DiLeu_BaEn_1 | 10 | 15 | PF01217 | 0.580 |
TRG_DiLeu_BaEn_1 | 40 | 45 | PF01217 | 0.487 |
TRG_DiLeu_BaLyEn_6 | 167 | 172 | PF01217 | 0.557 |
TRG_DiLeu_BaLyEn_6 | 253 | 258 | PF01217 | 0.639 |
TRG_DiLeu_BaLyEn_6 | 350 | 355 | PF01217 | 0.516 |
TRG_ER_diArg_1 | 133 | 135 | PF00400 | 0.490 |
TRG_ER_diArg_1 | 395 | 397 | PF00400 | 0.556 |
TRG_ER_diArg_1 | 85 | 87 | PF00400 | 0.455 |
TRG_Pf-PMV_PEXEL_1 | 180 | 184 | PF00026 | 0.700 |
TRG_Pf-PMV_PEXEL_1 | 373 | 378 | PF00026 | 0.532 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IIJ2 | Leptomonas seymouri | 36% | 87% |
A0A3Q8ILA1 | Leishmania donovani | 89% | 100% |
A4HPS7 | Leishmania braziliensis | 68% | 100% |
A4IE65 | Leishmania infantum | 89% | 100% |
E9ATJ2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |