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: 1, no: 7 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: A4HWA4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 240 | 244 | PF00656 | 0.519 |
CLV_C14_Caspase3-7 | 93 | 97 | PF00656 | 0.459 |
CLV_MEL_PAP_1 | 121 | 127 | PF00089 | 0.506 |
CLV_NRD_NRD_1 | 183 | 185 | PF00675 | 0.743 |
CLV_NRD_NRD_1 | 284 | 286 | PF00675 | 0.547 |
CLV_NRD_NRD_1 | 34 | 36 | PF00675 | 0.456 |
CLV_NRD_NRD_1 | 354 | 356 | PF00675 | 0.526 |
CLV_NRD_NRD_1 | 426 | 428 | PF00675 | 0.500 |
CLV_PCSK_FUR_1 | 181 | 185 | PF00082 | 0.615 |
CLV_PCSK_KEX2_1 | 183 | 185 | PF00082 | 0.725 |
CLV_PCSK_KEX2_1 | 284 | 286 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 34 | 36 | PF00082 | 0.456 |
CLV_PCSK_KEX2_1 | 354 | 356 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 426 | 428 | PF00082 | 0.482 |
CLV_PCSK_PC7_1 | 350 | 356 | PF00082 | 0.496 |
DEG_APCC_DBOX_1 | 123 | 131 | PF00400 | 0.514 |
DEG_APCC_DBOX_1 | 425 | 433 | PF00400 | 0.360 |
DOC_CYCLIN_RxL_1 | 390 | 401 | PF00134 | 0.540 |
DOC_CYCLIN_yCln2_LP_2 | 450 | 456 | PF00134 | 0.547 |
DOC_MAPK_gen_1 | 354 | 361 | PF00069 | 0.546 |
DOC_USP7_MATH_1 | 165 | 169 | PF00917 | 0.653 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.739 |
DOC_USP7_MATH_1 | 190 | 194 | PF00917 | 0.749 |
DOC_USP7_MATH_1 | 198 | 202 | PF00917 | 0.791 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 219 | 223 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 237 | 241 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 461 | 465 | PF00917 | 0.736 |
DOC_WW_Pin1_4 | 144 | 149 | PF00397 | 0.749 |
DOC_WW_Pin1_4 | 161 | 166 | PF00397 | 0.715 |
DOC_WW_Pin1_4 | 168 | 173 | PF00397 | 0.784 |
DOC_WW_Pin1_4 | 210 | 215 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 449 | 454 | PF00397 | 0.513 |
LIG_14-3-3_CanoR_1 | 124 | 128 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 157 | 166 | PF00244 | 0.633 |
LIG_14-3-3_CanoR_1 | 224 | 233 | PF00244 | 0.737 |
LIG_14-3-3_CanoR_1 | 236 | 242 | PF00244 | 0.572 |
LIG_14-3-3_CanoR_1 | 34 | 42 | PF00244 | 0.435 |
LIG_eIF4E_1 | 443 | 449 | PF01652 | 0.440 |
LIG_EVH1_1 | 414 | 418 | PF00568 | 0.516 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.528 |
LIG_FHA_1 | 153 | 159 | PF00498 | 0.583 |
LIG_FHA_1 | 215 | 221 | PF00498 | 0.587 |
LIG_FHA_1 | 256 | 262 | PF00498 | 0.555 |
LIG_FHA_1 | 59 | 65 | PF00498 | 0.678 |
LIG_FHA_2 | 240 | 246 | PF00498 | 0.502 |
LIG_FHA_2 | 27 | 33 | PF00498 | 0.398 |
LIG_FHA_2 | 71 | 77 | PF00498 | 0.517 |
LIG_FHA_2 | 91 | 97 | PF00498 | 0.316 |
LIG_IBAR_NPY_1 | 264 | 266 | PF08397 | 0.552 |
LIG_LIR_Gen_1 | 90 | 95 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 419 | 425 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 90 | 94 | PF02991 | 0.502 |
LIG_RPA_C_Fungi | 350 | 362 | PF08784 | 0.612 |
LIG_SH2_NCK_1 | 443 | 447 | PF00017 | 0.433 |
LIG_SH2_STAP1 | 102 | 106 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 44 | 47 | PF00017 | 0.546 |
LIG_SH3_3 | 109 | 115 | PF00018 | 0.506 |
LIG_SH3_3 | 142 | 148 | PF00018 | 0.609 |
LIG_SH3_3 | 179 | 185 | PF00018 | 0.760 |
LIG_SH3_3 | 213 | 219 | PF00018 | 0.606 |
LIG_SH3_3 | 410 | 416 | PF00018 | 0.602 |
LIG_SH3_3 | 450 | 456 | PF00018 | 0.531 |
LIG_SH3_3 | 61 | 67 | PF00018 | 0.624 |
LIG_SUMO_SIM_anti_2 | 90 | 96 | PF11976 | 0.449 |
LIG_SUMO_SIM_par_1 | 444 | 452 | PF11976 | 0.481 |
LIG_TRAF2_1 | 385 | 388 | PF00917 | 0.628 |
LIG_TRAF2_1 | 398 | 401 | PF00917 | 0.486 |
LIG_TRAF2_1 | 83 | 86 | PF00917 | 0.621 |
LIG_WRC_WIRS_1 | 88 | 93 | PF05994 | 0.450 |
MOD_CK1_1 | 164 | 170 | PF00069 | 0.779 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.722 |
MOD_CK1_1 | 223 | 229 | PF00069 | 0.650 |
MOD_CK1_1 | 244 | 250 | PF00069 | 0.619 |
MOD_CK1_1 | 46 | 52 | PF00069 | 0.497 |
MOD_CK2_1 | 123 | 129 | PF00069 | 0.672 |
MOD_CK2_1 | 144 | 150 | PF00069 | 0.747 |
MOD_CK2_1 | 239 | 245 | PF00069 | 0.515 |
MOD_CK2_1 | 341 | 347 | PF00069 | 0.479 |
MOD_CK2_1 | 461 | 467 | PF00069 | 0.616 |
MOD_CK2_1 | 72 | 78 | PF00069 | 0.429 |
MOD_GlcNHglycan | 108 | 111 | PF01048 | 0.522 |
MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.664 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.699 |
MOD_GlcNHglycan | 254 | 258 | PF01048 | 0.551 |
MOD_GlcNHglycan | 422 | 425 | PF01048 | 0.498 |
MOD_GlcNHglycan | 444 | 447 | PF01048 | 0.499 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.467 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.452 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.689 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.628 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.772 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.690 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.756 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.595 |
MOD_GSK3_1 | 237 | 244 | PF00069 | 0.681 |
MOD_GSK3_1 | 374 | 381 | PF00069 | 0.529 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.465 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.672 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.423 |
MOD_NEK2_1 | 220 | 225 | PF00069 | 0.590 |
MOD_PIKK_1 | 176 | 182 | PF00454 | 0.617 |
MOD_PKA_1 | 34 | 40 | PF00069 | 0.402 |
MOD_PKA_2 | 123 | 129 | PF00069 | 0.586 |
MOD_PKA_2 | 156 | 162 | PF00069 | 0.675 |
MOD_PKA_2 | 191 | 197 | PF00069 | 0.726 |
MOD_PKA_2 | 208 | 214 | PF00069 | 0.733 |
MOD_PKA_2 | 223 | 229 | PF00069 | 0.717 |
MOD_PKA_2 | 34 | 40 | PF00069 | 0.483 |
MOD_PKA_2 | 374 | 380 | PF00069 | 0.592 |
MOD_Plk_1 | 244 | 250 | PF00069 | 0.531 |
MOD_Plk_2-3 | 123 | 129 | PF00069 | 0.621 |
MOD_Plk_2-3 | 98 | 104 | PF00069 | 0.477 |
MOD_Plk_4 | 87 | 93 | PF00069 | 0.487 |
MOD_ProDKin_1 | 144 | 150 | PF00069 | 0.749 |
MOD_ProDKin_1 | 161 | 167 | PF00069 | 0.716 |
MOD_ProDKin_1 | 168 | 174 | PF00069 | 0.784 |
MOD_ProDKin_1 | 210 | 216 | PF00069 | 0.643 |
MOD_ProDKin_1 | 449 | 455 | PF00069 | 0.520 |
MOD_SUMO_for_1 | 7 | 10 | PF00179 | 0.475 |
TRG_DiLeu_BaEn_3 | 86 | 92 | PF01217 | 0.443 |
TRG_DiLeu_BaLyEn_6 | 390 | 395 | PF01217 | 0.465 |
TRG_ER_diArg_1 | 181 | 184 | PF00400 | 0.664 |
TRG_ER_diArg_1 | 284 | 286 | PF00400 | 0.456 |
TRG_ER_diArg_1 | 33 | 35 | PF00400 | 0.457 |
TRG_ER_diArg_1 | 425 | 427 | PF00400 | 0.474 |
TRG_Pf-PMV_PEXEL_1 | 277 | 282 | PF00026 | 0.446 |
TRG_Pf-PMV_PEXEL_1 | 34 | 38 | PF00026 | 0.451 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5C4 | Leptomonas seymouri | 40% | 87% |
A0A3Q8IIJ0 | Leishmania donovani | 100% | 100% |
A0A422NS55 | Trypanosoma rangeli | 31% | 78% |
A4H7X7 | Leishmania braziliensis | 64% | 100% |
C9ZNT9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 87% |
E9AQ04 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
Q4QFH7 | Leishmania major | 89% | 100% |