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: 3 |
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: Q4QHY1
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 8 |
GO:0003677 | DNA binding | 4 | 8 |
GO:0005488 | binding | 1 | 8 |
GO:0097159 | organic cyclic compound binding | 2 | 8 |
GO:1901363 | heterocyclic compound binding | 2 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 226 | 230 | PF00656 | 0.628 |
CLV_NRD_NRD_1 | 201 | 203 | PF00675 | 0.603 |
CLV_NRD_NRD_1 | 233 | 235 | PF00675 | 0.598 |
CLV_NRD_NRD_1 | 368 | 370 | PF00675 | 0.474 |
CLV_PCSK_FUR_1 | 199 | 203 | PF00082 | 0.599 |
CLV_PCSK_KEX2_1 | 14 | 16 | PF00082 | 0.351 |
CLV_PCSK_KEX2_1 | 201 | 203 | PF00082 | 0.603 |
CLV_PCSK_KEX2_1 | 233 | 235 | PF00082 | 0.598 |
CLV_PCSK_KEX2_1 | 368 | 370 | PF00082 | 0.474 |
CLV_PCSK_PC1ET2_1 | 14 | 16 | PF00082 | 0.351 |
CLV_PCSK_SKI1_1 | 136 | 140 | PF00082 | 0.426 |
CLV_PCSK_SKI1_1 | 319 | 323 | PF00082 | 0.692 |
CLV_PCSK_SKI1_1 | 352 | 356 | PF00082 | 0.607 |
CLV_PCSK_SKI1_1 | 42 | 46 | PF00082 | 0.292 |
DEG_COP1_1 | 124 | 132 | PF00400 | 0.447 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.508 |
DEG_SPOP_SBC_1 | 344 | 348 | PF00917 | 0.662 |
DOC_CYCLIN_RxL_1 | 39 | 49 | PF00134 | 0.292 |
DOC_CYCLIN_yCln2_LP_2 | 213 | 216 | PF00134 | 0.651 |
DOC_CYCLIN_yCln2_LP_2 | 87 | 93 | PF00134 | 0.357 |
DOC_MAPK_MEF2A_6 | 122 | 129 | PF00069 | 0.436 |
DOC_PP2B_LxvP_1 | 127 | 130 | PF13499 | 0.551 |
DOC_PP2B_LxvP_1 | 213 | 216 | PF13499 | 0.651 |
DOC_PP2B_LxvP_1 | 445 | 448 | PF13499 | 0.292 |
DOC_PP2B_LxvP_1 | 45 | 48 | PF13499 | 0.351 |
DOC_PP2B_LxvP_1 | 85 | 88 | PF13499 | 0.292 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 16 | 20 | PF00917 | 0.444 |
DOC_USP7_MATH_1 | 206 | 210 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 251 | 255 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 301 | 305 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 334 | 338 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 345 | 349 | PF00917 | 0.531 |
LIG_14-3-3_CanoR_1 | 20 | 27 | PF00244 | 0.351 |
LIG_14-3-3_CanoR_1 | 201 | 206 | PF00244 | 0.564 |
LIG_14-3-3_CanoR_1 | 233 | 240 | PF00244 | 0.609 |
LIG_14-3-3_CanoR_1 | 352 | 357 | PF00244 | 0.606 |
LIG_14-3-3_CanoR_1 | 58 | 68 | PF00244 | 0.357 |
LIG_BRCT_BRCA1_1 | 6 | 10 | PF00533 | 0.434 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.460 |
LIG_FHA_1 | 137 | 143 | PF00498 | 0.467 |
LIG_FHA_1 | 209 | 215 | PF00498 | 0.610 |
LIG_FHA_1 | 429 | 435 | PF00498 | 0.361 |
LIG_FHA_1 | 450 | 456 | PF00498 | 0.328 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.390 |
LIG_FHA_2 | 47 | 53 | PF00498 | 0.444 |
LIG_FHA_2 | 61 | 67 | PF00498 | 0.255 |
LIG_Integrin_isoDGR_2 | 165 | 167 | PF01839 | 0.603 |
LIG_LIR_Gen_1 | 116 | 125 | PF02991 | 0.391 |
LIG_LIR_Gen_1 | 79 | 90 | PF02991 | 0.313 |
LIG_LIR_Nem_3 | 66 | 71 | PF02991 | 0.314 |
LIG_LIR_Nem_3 | 79 | 85 | PF02991 | 0.313 |
LIG_PDZ_Class_3 | 464 | 469 | PF00595 | 0.512 |
LIG_SH2_NCK_1 | 306 | 310 | PF00017 | 0.685 |
LIG_SH2_STAT5 | 306 | 309 | PF00017 | 0.704 |
LIG_SH2_STAT5 | 407 | 410 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 54 | 57 | PF00017 | 0.292 |
LIG_SH2_STAT5 | 82 | 85 | PF00017 | 0.313 |
LIG_SH3_3 | 174 | 180 | PF00018 | 0.638 |
LIG_SH3_3 | 295 | 301 | PF00018 | 0.563 |
LIG_SH3_3 | 380 | 386 | PF00018 | 0.476 |
LIG_SH3_3 | 445 | 451 | PF00018 | 0.357 |
LIG_SUMO_SIM_anti_2 | 431 | 436 | PF11976 | 0.351 |
LIG_TRAF2_1 | 312 | 315 | PF00917 | 0.612 |
MOD_CK1_1 | 105 | 111 | PF00069 | 0.296 |
MOD_CK1_1 | 19 | 25 | PF00069 | 0.409 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.644 |
MOD_CK1_1 | 253 | 259 | PF00069 | 0.676 |
MOD_CK1_1 | 304 | 310 | PF00069 | 0.653 |
MOD_CK1_1 | 348 | 354 | PF00069 | 0.774 |
MOD_CK1_1 | 449 | 455 | PF00069 | 0.341 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.351 |
MOD_CK2_1 | 105 | 111 | PF00069 | 0.296 |
MOD_CK2_1 | 293 | 299 | PF00069 | 0.689 |
MOD_CK2_1 | 309 | 315 | PF00069 | 0.634 |
MOD_CK2_1 | 46 | 52 | PF00069 | 0.444 |
MOD_CK2_1 | 60 | 66 | PF00069 | 0.255 |
MOD_GlcNHglycan | 156 | 159 | PF01048 | 0.629 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.625 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.689 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.595 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.499 |
MOD_GlcNHglycan | 252 | 256 | PF01048 | 0.624 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.351 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.305 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.588 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.563 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.626 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.717 |
MOD_GSK3_1 | 289 | 296 | PF00069 | 0.701 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.633 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.361 |
MOD_N-GLC_1 | 105 | 110 | PF02516 | 0.319 |
MOD_N-GLC_1 | 158 | 163 | PF02516 | 0.717 |
MOD_N-GLC_1 | 30 | 35 | PF02516 | 0.313 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.581 |
MOD_NEK2_1 | 205 | 210 | PF00069 | 0.633 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.662 |
MOD_NEK2_1 | 343 | 348 | PF00069 | 0.656 |
MOD_NEK2_2 | 301 | 306 | PF00069 | 0.609 |
MOD_OFUCOSY | 443 | 450 | PF10250 | 0.365 |
MOD_PIKK_1 | 206 | 212 | PF00454 | 0.655 |
MOD_PIKK_1 | 309 | 315 | PF00454 | 0.639 |
MOD_PKA_1 | 201 | 207 | PF00069 | 0.601 |
MOD_PKA_1 | 233 | 239 | PF00069 | 0.590 |
MOD_PKA_2 | 19 | 25 | PF00069 | 0.351 |
MOD_PKA_2 | 201 | 207 | PF00069 | 0.565 |
MOD_PKA_2 | 232 | 238 | PF00069 | 0.656 |
MOD_PKB_1 | 199 | 207 | PF00069 | 0.599 |
MOD_Plk_1 | 105 | 111 | PF00069 | 0.338 |
MOD_Plk_1 | 30 | 36 | PF00069 | 0.313 |
MOD_Plk_1 | 4 | 10 | PF00069 | 0.450 |
MOD_Plk_4 | 208 | 214 | PF00069 | 0.608 |
MOD_Plk_4 | 272 | 278 | PF00069 | 0.667 |
MOD_Plk_4 | 301 | 307 | PF00069 | 0.647 |
MOD_Plk_4 | 345 | 351 | PF00069 | 0.788 |
MOD_Plk_4 | 428 | 434 | PF00069 | 0.305 |
TRG_DiLeu_BaLyEn_6 | 395 | 400 | PF01217 | 0.496 |
TRG_ENDOCYTIC_2 | 68 | 71 | PF00928 | 0.314 |
TRG_ENDOCYTIC_2 | 82 | 85 | PF00928 | 0.313 |
TRG_ER_diArg_1 | 199 | 202 | PF00400 | 0.603 |
TRG_ER_diArg_1 | 232 | 234 | PF00400 | 0.602 |
TRG_ER_diArg_1 | 368 | 371 | PF00400 | 0.532 |
TRG_ER_diArg_1 | 396 | 399 | PF00400 | 0.500 |
TRG_Pf-PMV_PEXEL_1 | 368 | 372 | PF00026 | 0.472 |
TRG_Pf-PMV_PEXEL_1 | 398 | 403 | PF00026 | 0.480 |
TRG_Pf-PMV_PEXEL_1 | 42 | 46 | PF00026 | 0.292 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I698 | Leptomonas seymouri | 60% | 98% |
A0A3S5H6D0 | Leishmania donovani | 95% | 100% |
A4H5L9 | Leishmania braziliensis | 73% | 100% |
A4HTV7 | Leishmania infantum | 96% | 100% |
E9AMP4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 98% |
V5BIH0 | Trypanosoma cruzi | 37% | 100% |