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: Q4Q0G5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 239 | 243 | PF00656 | 0.648 |
CLV_C14_Caspase3-7 | 24 | 28 | PF00656 | 0.535 |
CLV_NRD_NRD_1 | 120 | 122 | PF00675 | 0.501 |
CLV_NRD_NRD_1 | 302 | 304 | PF00675 | 0.592 |
CLV_PCSK_KEX2_1 | 119 | 121 | PF00082 | 0.519 |
CLV_PCSK_KEX2_1 | 302 | 304 | PF00082 | 0.692 |
CLV_PCSK_SKI1_1 | 11 | 15 | PF00082 | 0.587 |
DEG_COP1_1 | 239 | 247 | PF00400 | 0.578 |
DOC_CKS1_1 | 244 | 249 | PF01111 | 0.676 |
DOC_CKS1_1 | 270 | 275 | PF01111 | 0.564 |
DOC_MAPK_MEF2A_6 | 200 | 207 | PF00069 | 0.571 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.480 |
DOC_USP7_MATH_1 | 229 | 233 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.546 |
DOC_USP7_MATH_1 | 311 | 315 | PF00917 | 0.661 |
DOC_USP7_MATH_1 | 385 | 389 | PF00917 | 0.607 |
DOC_WW_Pin1_4 | 177 | 182 | PF00397 | 0.661 |
DOC_WW_Pin1_4 | 225 | 230 | PF00397 | 0.760 |
DOC_WW_Pin1_4 | 243 | 248 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 269 | 274 | PF00397 | 0.585 |
DOC_WW_Pin1_4 | 307 | 312 | PF00397 | 0.641 |
DOC_WW_Pin1_4 | 41 | 46 | PF00397 | 0.627 |
DOC_WW_Pin1_4 | 73 | 78 | PF00397 | 0.486 |
LIG_14-3-3_CanoR_1 | 155 | 160 | PF00244 | 0.637 |
LIG_14-3-3_CanoR_1 | 80 | 87 | PF00244 | 0.542 |
LIG_BIR_III_4 | 186 | 190 | PF00653 | 0.598 |
LIG_BRCT_BRCA1_1 | 215 | 219 | PF00533 | 0.516 |
LIG_DLG_GKlike_1 | 155 | 163 | PF00625 | 0.613 |
LIG_FHA_1 | 190 | 196 | PF00498 | 0.591 |
LIG_FHA_1 | 199 | 205 | PF00498 | 0.530 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.674 |
LIG_FHA_1 | 310 | 316 | PF00498 | 0.591 |
LIG_FHA_1 | 338 | 344 | PF00498 | 0.581 |
LIG_FHA_2 | 112 | 118 | PF00498 | 0.522 |
LIG_FHA_2 | 215 | 221 | PF00498 | 0.574 |
LIG_FHA_2 | 253 | 259 | PF00498 | 0.578 |
LIG_FHA_2 | 74 | 80 | PF00498 | 0.453 |
LIG_LIR_Gen_1 | 216 | 227 | PF02991 | 0.557 |
LIG_LIR_Nem_3 | 146 | 152 | PF02991 | 0.548 |
LIG_LIR_Nem_3 | 216 | 222 | PF02991 | 0.552 |
LIG_MYND_3 | 320 | 324 | PF01753 | 0.576 |
LIG_Pex14_2 | 219 | 223 | PF04695 | 0.561 |
LIG_Pex14_2 | 68 | 72 | PF04695 | 0.537 |
LIG_PTAP_UEV_1 | 246 | 251 | PF05743 | 0.622 |
LIG_Rb_pABgroove_1 | 363 | 371 | PF01858 | 0.441 |
LIG_SH2_STAP1 | 371 | 375 | PF00017 | 0.536 |
LIG_SH3_2 | 178 | 183 | PF14604 | 0.548 |
LIG_SH3_3 | 175 | 181 | PF00018 | 0.555 |
LIG_SH3_3 | 241 | 247 | PF00018 | 0.588 |
LIG_SH3_3 | 267 | 273 | PF00018 | 0.652 |
LIG_SH3_3 | 305 | 311 | PF00018 | 0.656 |
LIG_SH3_3 | 315 | 321 | PF00018 | 0.546 |
LIG_SH3_5 | 367 | 371 | PF00018 | 0.451 |
LIG_SUMO_SIM_par_1 | 191 | 199 | PF11976 | 0.583 |
LIG_TRAF2_1 | 60 | 63 | PF00917 | 0.532 |
LIG_TRFH_1 | 363 | 367 | PF08558 | 0.481 |
MOD_CDC14_SPxK_1 | 180 | 183 | PF00782 | 0.635 |
MOD_CDK_SPxK_1 | 177 | 183 | PF00069 | 0.636 |
MOD_CDK_SPxxK_3 | 73 | 80 | PF00069 | 0.476 |
MOD_CK1_1 | 151 | 157 | PF00069 | 0.683 |
MOD_CK1_1 | 158 | 164 | PF00069 | 0.725 |
MOD_CK1_1 | 179 | 185 | PF00069 | 0.654 |
MOD_CK1_1 | 198 | 204 | PF00069 | 0.465 |
MOD_CK1_1 | 232 | 238 | PF00069 | 0.548 |
MOD_CK1_1 | 275 | 281 | PF00069 | 0.683 |
MOD_CK1_1 | 306 | 312 | PF00069 | 0.604 |
MOD_CK1_1 | 314 | 320 | PF00069 | 0.595 |
MOD_CK1_1 | 337 | 343 | PF00069 | 0.558 |
MOD_CK1_1 | 43 | 49 | PF00069 | 0.588 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.557 |
MOD_CK2_1 | 111 | 117 | PF00069 | 0.530 |
MOD_CK2_1 | 252 | 258 | PF00069 | 0.581 |
MOD_CK2_1 | 310 | 316 | PF00069 | 0.594 |
MOD_CK2_1 | 57 | 63 | PF00069 | 0.517 |
MOD_GlcNHglycan | 138 | 141 | PF01048 | 0.520 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.625 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.575 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.621 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.791 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.594 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.454 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.617 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.642 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.634 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.608 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.578 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.493 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.633 |
MOD_NEK2_1 | 195 | 200 | PF00069 | 0.528 |
MOD_PIKK_1 | 278 | 284 | PF00454 | 0.674 |
MOD_PIKK_1 | 47 | 53 | PF00454 | 0.465 |
MOD_PKA_2 | 136 | 142 | PF00069 | 0.570 |
MOD_PKA_2 | 337 | 343 | PF00069 | 0.624 |
MOD_PKA_2 | 79 | 85 | PF00069 | 0.528 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.560 |
MOD_ProDKin_1 | 177 | 183 | PF00069 | 0.660 |
MOD_ProDKin_1 | 225 | 231 | PF00069 | 0.764 |
MOD_ProDKin_1 | 243 | 249 | PF00069 | 0.543 |
MOD_ProDKin_1 | 269 | 275 | PF00069 | 0.586 |
MOD_ProDKin_1 | 307 | 313 | PF00069 | 0.641 |
MOD_ProDKin_1 | 41 | 47 | PF00069 | 0.621 |
MOD_ProDKin_1 | 73 | 79 | PF00069 | 0.485 |
MOD_SUMO_for_1 | 85 | 88 | PF00179 | 0.576 |
TRG_DiLeu_BaEn_2 | 340 | 346 | PF01217 | 0.545 |
TRG_ER_diArg_1 | 118 | 121 | PF00400 | 0.479 |
TRG_Pf-PMV_PEXEL_1 | 120 | 124 | PF00026 | 0.513 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P903 | Leptomonas seymouri | 35% | 100% |
A0A3Q8IGQ8 | Leishmania donovani | 83% | 100% |
A4HQB4 | Leishmania braziliensis | 51% | 100% |
A4IE08 | Leishmania infantum | 83% | 100% |
E9AU30 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |