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: A0A3Q8IIJ0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 240 | 244 | PF00656 | 0.660 |
CLV_C14_Caspase3-7 | 93 | 97 | PF00656 | 0.587 |
CLV_MEL_PAP_1 | 121 | 127 | PF00089 | 0.565 |
CLV_NRD_NRD_1 | 183 | 185 | PF00675 | 0.798 |
CLV_NRD_NRD_1 | 284 | 286 | PF00675 | 0.605 |
CLV_NRD_NRD_1 | 34 | 36 | PF00675 | 0.577 |
CLV_NRD_NRD_1 | 354 | 356 | PF00675 | 0.567 |
CLV_NRD_NRD_1 | 426 | 428 | PF00675 | 0.542 |
CLV_PCSK_FUR_1 | 181 | 185 | PF00082 | 0.743 |
CLV_PCSK_KEX2_1 | 183 | 185 | PF00082 | 0.771 |
CLV_PCSK_KEX2_1 | 284 | 286 | PF00082 | 0.602 |
CLV_PCSK_KEX2_1 | 34 | 36 | PF00082 | 0.535 |
CLV_PCSK_KEX2_1 | 354 | 356 | PF00082 | 0.584 |
CLV_PCSK_KEX2_1 | 426 | 428 | PF00082 | 0.530 |
CLV_PCSK_PC7_1 | 350 | 356 | PF00082 | 0.559 |
DEG_APCC_DBOX_1 | 123 | 131 | PF00400 | 0.573 |
DEG_APCC_DBOX_1 | 425 | 433 | PF00400 | 0.412 |
DOC_CYCLIN_RxL_1 | 390 | 401 | PF00134 | 0.605 |
DOC_CYCLIN_yCln2_LP_2 | 450 | 456 | PF00134 | 0.692 |
DOC_MAPK_gen_1 | 354 | 361 | PF00069 | 0.603 |
DOC_USP7_MATH_1 | 165 | 169 | PF00917 | 0.765 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.750 |
DOC_USP7_MATH_1 | 190 | 194 | PF00917 | 0.596 |
DOC_USP7_MATH_1 | 198 | 202 | PF00917 | 0.773 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 219 | 223 | PF00917 | 0.724 |
DOC_USP7_MATH_1 | 237 | 241 | PF00917 | 0.743 |
DOC_USP7_MATH_1 | 461 | 465 | PF00917 | 0.811 |
DOC_WW_Pin1_4 | 144 | 149 | PF00397 | 0.711 |
DOC_WW_Pin1_4 | 161 | 166 | PF00397 | 0.659 |
DOC_WW_Pin1_4 | 168 | 173 | PF00397 | 0.786 |
DOC_WW_Pin1_4 | 210 | 215 | PF00397 | 0.721 |
DOC_WW_Pin1_4 | 449 | 454 | PF00397 | 0.623 |
LIG_14-3-3_CanoR_1 | 124 | 128 | PF00244 | 0.574 |
LIG_14-3-3_CanoR_1 | 157 | 166 | PF00244 | 0.635 |
LIG_14-3-3_CanoR_1 | 224 | 233 | PF00244 | 0.721 |
LIG_14-3-3_CanoR_1 | 236 | 242 | PF00244 | 0.714 |
LIG_14-3-3_CanoR_1 | 34 | 42 | PF00244 | 0.640 |
LIG_14-3-3_CanoR_1 | 57 | 63 | PF00244 | 0.569 |
LIG_eIF4E_1 | 443 | 449 | PF01652 | 0.561 |
LIG_EVH1_1 | 414 | 418 | PF00568 | 0.624 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.639 |
LIG_FHA_1 | 153 | 159 | PF00498 | 0.624 |
LIG_FHA_1 | 215 | 221 | PF00498 | 0.679 |
LIG_FHA_1 | 256 | 262 | PF00498 | 0.611 |
LIG_FHA_1 | 59 | 65 | PF00498 | 0.686 |
LIG_FHA_2 | 240 | 246 | PF00498 | 0.588 |
LIG_FHA_2 | 27 | 33 | PF00498 | 0.513 |
LIG_FHA_2 | 71 | 77 | PF00498 | 0.584 |
LIG_FHA_2 | 91 | 97 | PF00498 | 0.427 |
LIG_IBAR_NPY_1 | 264 | 266 | PF08397 | 0.622 |
LIG_LIR_Gen_1 | 90 | 95 | PF02991 | 0.613 |
LIG_LIR_Nem_3 | 419 | 425 | PF02991 | 0.593 |
LIG_LIR_Nem_3 | 90 | 94 | PF02991 | 0.614 |
LIG_RPA_C_Fungi | 350 | 362 | PF08784 | 0.638 |
LIG_SH2_NCK_1 | 443 | 447 | PF00017 | 0.564 |
LIG_SH2_STAP1 | 102 | 106 | PF00017 | 0.600 |
LIG_SH2_STAT5 | 44 | 47 | PF00017 | 0.591 |
LIG_SH3_3 | 109 | 115 | PF00018 | 0.650 |
LIG_SH3_3 | 142 | 148 | PF00018 | 0.729 |
LIG_SH3_3 | 179 | 185 | PF00018 | 0.807 |
LIG_SH3_3 | 213 | 219 | PF00018 | 0.681 |
LIG_SH3_3 | 410 | 416 | PF00018 | 0.638 |
LIG_SH3_3 | 450 | 456 | PF00018 | 0.630 |
LIG_SH3_3 | 61 | 67 | PF00018 | 0.709 |
LIG_SUMO_SIM_anti_2 | 90 | 96 | PF11976 | 0.653 |
LIG_SUMO_SIM_par_1 | 444 | 452 | PF11976 | 0.630 |
LIG_TRAF2_1 | 385 | 388 | PF00917 | 0.677 |
LIG_TRAF2_1 | 398 | 401 | PF00917 | 0.564 |
LIG_TRAF2_1 | 83 | 86 | PF00917 | 0.645 |
LIG_WRC_WIRS_1 | 88 | 93 | PF05994 | 0.575 |
MOD_CK1_1 | 164 | 170 | PF00069 | 0.765 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.760 |
MOD_CK1_1 | 223 | 229 | PF00069 | 0.676 |
MOD_CK1_1 | 244 | 250 | PF00069 | 0.665 |
MOD_CK1_1 | 46 | 52 | PF00069 | 0.697 |
MOD_CK2_1 | 123 | 129 | PF00069 | 0.739 |
MOD_CK2_1 | 144 | 150 | PF00069 | 0.710 |
MOD_CK2_1 | 239 | 245 | PF00069 | 0.601 |
MOD_CK2_1 | 341 | 347 | PF00069 | 0.550 |
MOD_CK2_1 | 461 | 467 | PF00069 | 0.741 |
MOD_CK2_1 | 72 | 78 | PF00069 | 0.485 |
MOD_GlcNHglycan | 108 | 111 | PF01048 | 0.643 |
MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.699 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.737 |
MOD_GlcNHglycan | 254 | 258 | PF01048 | 0.676 |
MOD_GlcNHglycan | 422 | 425 | PF01048 | 0.652 |
MOD_GlcNHglycan | 444 | 447 | PF01048 | 0.581 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.596 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.651 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.700 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.659 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.752 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.562 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.714 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.747 |
MOD_GSK3_1 | 237 | 244 | PF00069 | 0.714 |
MOD_GSK3_1 | 374 | 381 | PF00069 | 0.589 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.649 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.582 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.577 |
MOD_NEK2_1 | 220 | 225 | PF00069 | 0.767 |
MOD_PIKK_1 | 176 | 182 | PF00454 | 0.804 |
MOD_PKA_1 | 34 | 40 | PF00069 | 0.573 |
MOD_PKA_2 | 123 | 129 | PF00069 | 0.661 |
MOD_PKA_2 | 156 | 162 | PF00069 | 0.718 |
MOD_PKA_2 | 191 | 197 | PF00069 | 0.827 |
MOD_PKA_2 | 208 | 214 | PF00069 | 0.772 |
MOD_PKA_2 | 223 | 229 | PF00069 | 0.725 |
MOD_PKA_2 | 34 | 40 | PF00069 | 0.602 |
MOD_PKA_2 | 374 | 380 | PF00069 | 0.649 |
MOD_Plk_1 | 244 | 250 | PF00069 | 0.605 |
MOD_Plk_2-3 | 123 | 129 | PF00069 | 0.764 |
MOD_Plk_2-3 | 98 | 104 | PF00069 | 0.566 |
MOD_Plk_4 | 87 | 93 | PF00069 | 0.576 |
MOD_ProDKin_1 | 144 | 150 | PF00069 | 0.710 |
MOD_ProDKin_1 | 161 | 167 | PF00069 | 0.661 |
MOD_ProDKin_1 | 168 | 174 | PF00069 | 0.787 |
MOD_ProDKin_1 | 210 | 216 | PF00069 | 0.720 |
MOD_ProDKin_1 | 449 | 455 | PF00069 | 0.628 |
MOD_SUMO_for_1 | 7 | 10 | PF00179 | 0.619 |
TRG_DiLeu_BaEn_3 | 86 | 92 | PF01217 | 0.603 |
TRG_DiLeu_BaLyEn_6 | 390 | 395 | PF01217 | 0.580 |
TRG_ER_diArg_1 | 181 | 184 | PF00400 | 0.822 |
TRG_ER_diArg_1 | 284 | 286 | PF00400 | 0.503 |
TRG_ER_diArg_1 | 33 | 35 | PF00400 | 0.571 |
TRG_ER_diArg_1 | 425 | 427 | PF00400 | 0.548 |
TRG_Pf-PMV_PEXEL_1 | 277 | 282 | PF00026 | 0.559 |
TRG_Pf-PMV_PEXEL_1 | 34 | 38 | PF00026 | 0.583 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5C4 | Leptomonas seymouri | 40% | 87% |
A0A422NS55 | Trypanosoma rangeli | 31% | 78% |
A4H7X7 | Leishmania braziliensis | 64% | 100% |
A4HWA4 | Leishmania infantum | 100% | 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% |