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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: Q4QFH7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 240 | 244 | PF00656 | 0.544 |
CLV_C14_Caspase3-7 | 93 | 97 | PF00656 | 0.504 |
CLV_NRD_NRD_1 | 183 | 185 | PF00675 | 0.671 |
CLV_NRD_NRD_1 | 284 | 286 | PF00675 | 0.536 |
CLV_NRD_NRD_1 | 34 | 36 | PF00675 | 0.460 |
CLV_NRD_NRD_1 | 354 | 356 | PF00675 | 0.498 |
CLV_NRD_NRD_1 | 426 | 428 | PF00675 | 0.460 |
CLV_PCSK_FUR_1 | 181 | 185 | PF00082 | 0.627 |
CLV_PCSK_KEX2_1 | 183 | 185 | PF00082 | 0.632 |
CLV_PCSK_KEX2_1 | 284 | 286 | PF00082 | 0.552 |
CLV_PCSK_KEX2_1 | 34 | 36 | PF00082 | 0.460 |
CLV_PCSK_KEX2_1 | 354 | 356 | PF00082 | 0.498 |
CLV_PCSK_KEX2_1 | 426 | 428 | PF00082 | 0.460 |
CLV_PCSK_PC7_1 | 350 | 356 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 300 | 304 | PF00082 | 0.624 |
DOC_CYCLIN_RxL_1 | 390 | 401 | PF00134 | 0.507 |
DOC_CYCLIN_yCln2_LP_2 | 450 | 456 | PF00134 | 0.557 |
DOC_MAPK_gen_1 | 354 | 361 | PF00069 | 0.506 |
DOC_USP7_MATH_1 | 165 | 169 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 190 | 194 | PF00917 | 0.493 |
DOC_USP7_MATH_1 | 198 | 202 | PF00917 | 0.796 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 237 | 241 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 461 | 465 | PF00917 | 0.651 |
DOC_WW_Pin1_4 | 144 | 149 | PF00397 | 0.619 |
DOC_WW_Pin1_4 | 161 | 166 | PF00397 | 0.518 |
DOC_WW_Pin1_4 | 168 | 173 | PF00397 | 0.559 |
DOC_WW_Pin1_4 | 210 | 215 | PF00397 | 0.619 |
DOC_WW_Pin1_4 | 443 | 448 | PF00397 | 0.481 |
DOC_WW_Pin1_4 | 449 | 454 | PF00397 | 0.570 |
LIG_14-3-3_CanoR_1 | 224 | 233 | PF00244 | 0.613 |
LIG_14-3-3_CanoR_1 | 236 | 242 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 34 | 42 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 43 | 49 | PF00244 | 0.406 |
LIG_14-3-3_CanoR_1 | 68 | 77 | PF00244 | 0.726 |
LIG_eIF4E_1 | 443 | 449 | PF01652 | 0.464 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.495 |
LIG_FHA_1 | 215 | 221 | PF00498 | 0.581 |
LIG_FHA_1 | 225 | 231 | PF00498 | 0.523 |
LIG_FHA_1 | 256 | 262 | PF00498 | 0.506 |
LIG_FHA_1 | 305 | 311 | PF00498 | 0.546 |
LIG_FHA_1 | 319 | 325 | PF00498 | 0.404 |
LIG_FHA_1 | 444 | 450 | PF00498 | 0.410 |
LIG_FHA_2 | 240 | 246 | PF00498 | 0.552 |
LIG_FHA_2 | 27 | 33 | PF00498 | 0.430 |
LIG_FHA_2 | 318 | 324 | PF00498 | 0.404 |
LIG_FHA_2 | 71 | 77 | PF00498 | 0.628 |
LIG_FHA_2 | 91 | 97 | PF00498 | 0.447 |
LIG_LIR_Gen_1 | 419 | 429 | PF02991 | 0.407 |
LIG_LIR_Gen_1 | 90 | 95 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 419 | 425 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 90 | 94 | PF02991 | 0.519 |
LIG_RPA_C_Fungi | 350 | 362 | PF08784 | 0.587 |
LIG_SH2_NCK_1 | 48 | 52 | PF00017 | 0.410 |
LIG_SH2_STAP1 | 102 | 106 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 266 | 269 | PF00017 | 0.493 |
LIG_SH2_STAT5 | 44 | 47 | PF00017 | 0.538 |
LIG_SH3_2 | 231 | 236 | PF14604 | 0.484 |
LIG_SH3_3 | 109 | 115 | PF00018 | 0.569 |
LIG_SH3_3 | 142 | 148 | PF00018 | 0.621 |
LIG_SH3_3 | 179 | 185 | PF00018 | 0.733 |
LIG_SH3_3 | 228 | 234 | PF00018 | 0.505 |
LIG_SH3_3 | 410 | 416 | PF00018 | 0.546 |
LIG_SH3_3 | 64 | 70 | PF00018 | 0.643 |
LIG_SUMO_SIM_anti_2 | 90 | 96 | PF11976 | 0.504 |
LIG_SUMO_SIM_par_1 | 444 | 452 | PF11976 | 0.502 |
LIG_TRAF2_1 | 385 | 388 | PF00917 | 0.605 |
LIG_TRAF2_1 | 398 | 401 | PF00917 | 0.457 |
LIG_TRAF2_1 | 83 | 86 | PF00917 | 0.641 |
LIG_WRC_WIRS_1 | 88 | 93 | PF05994 | 0.461 |
MOD_CK1_1 | 164 | 170 | PF00069 | 0.649 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.630 |
MOD_CK1_1 | 223 | 229 | PF00069 | 0.571 |
MOD_CK1_1 | 244 | 250 | PF00069 | 0.612 |
MOD_CK1_1 | 46 | 52 | PF00069 | 0.528 |
MOD_CK2_1 | 123 | 129 | PF00069 | 0.658 |
MOD_CK2_1 | 144 | 150 | PF00069 | 0.618 |
MOD_CK2_1 | 239 | 245 | PF00069 | 0.565 |
MOD_CK2_1 | 341 | 347 | PF00069 | 0.477 |
MOD_CK2_1 | 461 | 467 | PF00069 | 0.625 |
MOD_GlcNHglycan | 108 | 111 | PF01048 | 0.542 |
MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.647 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.598 |
MOD_GlcNHglycan | 254 | 258 | PF01048 | 0.535 |
MOD_GlcNHglycan | 422 | 425 | PF01048 | 0.534 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.522 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.489 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.681 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.622 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.655 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.567 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.543 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.717 |
MOD_GSK3_1 | 237 | 244 | PF00069 | 0.698 |
MOD_GSK3_1 | 374 | 381 | PF00069 | 0.480 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.490 |
MOD_GSK3_1 | 439 | 446 | PF00069 | 0.512 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.521 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.579 |
MOD_PIKK_1 | 176 | 182 | PF00454 | 0.628 |
MOD_PKA_1 | 34 | 40 | PF00069 | 0.441 |
MOD_PKA_2 | 191 | 197 | PF00069 | 0.721 |
MOD_PKA_2 | 208 | 214 | PF00069 | 0.539 |
MOD_PKA_2 | 223 | 229 | PF00069 | 0.597 |
MOD_PKA_2 | 317 | 323 | PF00069 | 0.449 |
MOD_PKA_2 | 34 | 40 | PF00069 | 0.485 |
MOD_PKA_2 | 374 | 380 | PF00069 | 0.537 |
MOD_Plk_1 | 244 | 250 | PF00069 | 0.507 |
MOD_Plk_2-3 | 123 | 129 | PF00069 | 0.641 |
MOD_Plk_2-3 | 98 | 104 | PF00069 | 0.482 |
MOD_Plk_4 | 87 | 93 | PF00069 | 0.462 |
MOD_ProDKin_1 | 144 | 150 | PF00069 | 0.618 |
MOD_ProDKin_1 | 161 | 167 | PF00069 | 0.518 |
MOD_ProDKin_1 | 168 | 174 | PF00069 | 0.560 |
MOD_ProDKin_1 | 210 | 216 | PF00069 | 0.619 |
MOD_ProDKin_1 | 443 | 449 | PF00069 | 0.489 |
MOD_SUMO_for_1 | 7 | 10 | PF00179 | 0.506 |
TRG_DiLeu_BaEn_3 | 86 | 92 | PF01217 | 0.486 |
TRG_DiLeu_BaLyEn_6 | 215 | 220 | PF01217 | 0.514 |
TRG_DiLeu_BaLyEn_6 | 390 | 395 | PF01217 | 0.462 |
TRG_ER_diArg_1 | 181 | 184 | PF00400 | 0.684 |
TRG_ER_diArg_1 | 284 | 286 | PF00400 | 0.469 |
TRG_ER_diArg_1 | 33 | 35 | PF00400 | 0.452 |
TRG_ER_diArg_1 | 425 | 427 | PF00400 | 0.463 |
TRG_ER_diArg_1 | 66 | 69 | PF00400 | 0.537 |
TRG_Pf-PMV_PEXEL_1 | 277 | 282 | PF00026 | 0.460 |
TRG_Pf-PMV_PEXEL_1 | 34 | 38 | PF00026 | 0.463 |
TRG_Pf-PMV_PEXEL_1 | 384 | 388 | PF00026 | 0.424 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5C4 | Leptomonas seymouri | 41% | 87% |
A0A3Q8IIJ0 | Leishmania donovani | 89% | 100% |
A0A422NS55 | Trypanosoma rangeli | 30% | 78% |
A4H7X7 | Leishmania braziliensis | 65% | 100% |
A4HWA4 | Leishmania infantum | 89% | 100% |
E9AQ04 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |