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: A4IE08
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 239 | 243 | PF00656 | 0.760 |
CLV_NRD_NRD_1 | 120 | 122 | PF00675 | 0.607 |
CLV_NRD_NRD_1 | 303 | 305 | PF00675 | 0.707 |
CLV_PCSK_KEX2_1 | 120 | 122 | PF00082 | 0.606 |
CLV_PCSK_KEX2_1 | 303 | 305 | PF00082 | 0.707 |
CLV_PCSK_PC7_1 | 299 | 305 | PF00082 | 0.607 |
CLV_PCSK_SKI1_1 | 11 | 15 | PF00082 | 0.658 |
DOC_CKS1_1 | 244 | 249 | PF01111 | 0.821 |
DOC_CYCLIN_RxL_1 | 125 | 136 | PF00134 | 0.460 |
DOC_MAPK_MEF2A_6 | 200 | 207 | PF00069 | 0.664 |
DOC_USP7_MATH_1 | 232 | 236 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.742 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.655 |
DOC_USP7_MATH_1 | 311 | 315 | PF00917 | 0.786 |
DOC_USP7_MATH_1 | 385 | 389 | PF00917 | 0.663 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.560 |
DOC_USP7_MATH_1 | 43 | 47 | PF00917 | 0.622 |
DOC_WW_Pin1_4 | 177 | 182 | PF00397 | 0.812 |
DOC_WW_Pin1_4 | 225 | 230 | PF00397 | 0.786 |
DOC_WW_Pin1_4 | 243 | 248 | PF00397 | 0.628 |
DOC_WW_Pin1_4 | 307 | 312 | PF00397 | 0.780 |
DOC_WW_Pin1_4 | 41 | 46 | PF00397 | 0.729 |
DOC_WW_Pin1_4 | 73 | 78 | PF00397 | 0.697 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.581 |
LIG_14-3-3_CanoR_1 | 155 | 160 | PF00244 | 0.699 |
LIG_14-3-3_CanoR_1 | 80 | 87 | PF00244 | 0.718 |
LIG_BIR_III_4 | 186 | 190 | PF00653 | 0.702 |
LIG_BRCT_BRCA1_1 | 215 | 219 | PF00533 | 0.622 |
LIG_DLG_GKlike_1 | 155 | 163 | PF00625 | 0.710 |
LIG_FHA_1 | 190 | 196 | PF00498 | 0.693 |
LIG_FHA_1 | 199 | 205 | PF00498 | 0.645 |
LIG_FHA_1 | 262 | 268 | PF00498 | 0.632 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.730 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.744 |
LIG_FHA_1 | 310 | 316 | PF00498 | 0.751 |
LIG_FHA_1 | 338 | 344 | PF00498 | 0.688 |
LIG_FHA_2 | 112 | 118 | PF00498 | 0.639 |
LIG_FHA_2 | 215 | 221 | PF00498 | 0.651 |
LIG_FHA_2 | 74 | 80 | PF00498 | 0.582 |
LIG_LIR_Gen_1 | 216 | 227 | PF02991 | 0.665 |
LIG_LIR_Nem_3 | 148 | 152 | PF02991 | 0.656 |
LIG_LIR_Nem_3 | 216 | 222 | PF02991 | 0.661 |
LIG_MYND_3 | 320 | 324 | PF01753 | 0.660 |
LIG_PCNA_yPIPBox_3 | 51 | 61 | PF02747 | 0.521 |
LIG_Pex14_2 | 219 | 223 | PF04695 | 0.670 |
LIG_Pex14_2 | 68 | 72 | PF04695 | 0.689 |
LIG_PTAP_UEV_1 | 246 | 251 | PF05743 | 0.734 |
LIG_Rb_pABgroove_1 | 363 | 371 | PF01858 | 0.581 |
LIG_SH2_CRK | 149 | 153 | PF00017 | 0.612 |
LIG_SH2_STAP1 | 371 | 375 | PF00017 | 0.705 |
LIG_SH2_STAT3 | 17 | 20 | PF00017 | 0.602 |
LIG_SH3_3 | 226 | 232 | PF00018 | 0.766 |
LIG_SH3_3 | 241 | 247 | PF00018 | 0.690 |
LIG_SH3_3 | 264 | 270 | PF00018 | 0.795 |
LIG_SH3_3 | 305 | 311 | PF00018 | 0.769 |
LIG_SH3_3 | 315 | 321 | PF00018 | 0.634 |
LIG_SH3_5 | 367 | 371 | PF00018 | 0.587 |
LIG_SUMO_SIM_par_1 | 191 | 197 | PF11976 | 0.666 |
LIG_TRAF2_1 | 60 | 63 | PF00917 | 0.638 |
LIG_TRAF2_1 | 89 | 92 | PF00917 | 0.562 |
LIG_TRFH_1 | 363 | 367 | PF08558 | 0.627 |
LIG_UBA3_1 | 252 | 258 | PF00899 | 0.559 |
MOD_CDC14_SPxK_1 | 180 | 183 | PF00782 | 0.729 |
MOD_CDK_SPxK_1 | 177 | 183 | PF00069 | 0.732 |
MOD_CDK_SPxxK_3 | 73 | 80 | PF00069 | 0.608 |
MOD_CK1_1 | 151 | 157 | PF00069 | 0.684 |
MOD_CK1_1 | 158 | 164 | PF00069 | 0.765 |
MOD_CK1_1 | 179 | 185 | PF00069 | 0.723 |
MOD_CK1_1 | 275 | 281 | PF00069 | 0.743 |
MOD_CK1_1 | 309 | 315 | PF00069 | 0.706 |
MOD_CK1_1 | 337 | 343 | PF00069 | 0.643 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.703 |
MOD_CK2_1 | 111 | 117 | PF00069 | 0.649 |
MOD_CK2_1 | 299 | 305 | PF00069 | 0.768 |
MOD_CK2_1 | 310 | 316 | PF00069 | 0.672 |
MOD_CK2_1 | 57 | 63 | PF00069 | 0.633 |
MOD_GlcNHglycan | 138 | 141 | PF01048 | 0.621 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.680 |
MOD_GlcNHglycan | 167 | 173 | PF01048 | 0.706 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.707 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.817 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.705 |
MOD_GlcNHglycan | 274 | 277 | PF01048 | 0.672 |
MOD_GlcNHglycan | 40 | 43 | PF01048 | 0.584 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.483 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.737 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.570 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.731 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.685 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.698 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.648 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.718 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.559 |
MOD_PIKK_1 | 278 | 284 | PF00454 | 0.824 |
MOD_PKA_2 | 136 | 142 | PF00069 | 0.608 |
MOD_PKA_2 | 337 | 343 | PF00069 | 0.759 |
MOD_PKA_2 | 79 | 85 | PF00069 | 0.706 |
MOD_PKB_1 | 304 | 312 | PF00069 | 0.642 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.707 |
MOD_ProDKin_1 | 177 | 183 | PF00069 | 0.812 |
MOD_ProDKin_1 | 225 | 231 | PF00069 | 0.786 |
MOD_ProDKin_1 | 243 | 249 | PF00069 | 0.624 |
MOD_ProDKin_1 | 307 | 313 | PF00069 | 0.776 |
MOD_ProDKin_1 | 41 | 47 | PF00069 | 0.724 |
MOD_ProDKin_1 | 73 | 79 | PF00069 | 0.696 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.584 |
MOD_SUMO_for_1 | 85 | 88 | PF00179 | 0.742 |
TRG_DiLeu_BaEn_2 | 340 | 346 | PF01217 | 0.637 |
TRG_ENDOCYTIC_2 | 149 | 152 | PF00928 | 0.611 |
TRG_ER_diArg_1 | 119 | 121 | PF00400 | 0.577 |
TRG_Pf-PMV_PEXEL_1 | 120 | 124 | PF00026 | 0.610 |
TRG_Pf-PMV_PEXEL_1 | 164 | 168 | PF00026 | 0.601 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P903 | Leptomonas seymouri | 34% | 100% |
A0A3Q8IGQ8 | Leishmania donovani | 99% | 100% |
A4HQB4 | Leishmania braziliensis | 52% | 99% |
E9AU30 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
Q4Q0G5 | Leishmania major | 83% | 100% |