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: Q4Q3G6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 169 | 173 | PF00656 | 0.557 |
CLV_C14_Caspase3-7 | 51 | 55 | PF00656 | 0.731 |
CLV_MEL_PAP_1 | 194 | 200 | PF00089 | 0.427 |
CLV_NRD_NRD_1 | 287 | 289 | PF00675 | 0.457 |
CLV_NRD_NRD_1 | 405 | 407 | PF00675 | 0.415 |
CLV_NRD_NRD_1 | 98 | 100 | PF00675 | 0.618 |
CLV_PCSK_FUR_1 | 285 | 289 | PF00082 | 0.438 |
CLV_PCSK_KEX2_1 | 285 | 287 | PF00082 | 0.434 |
CLV_PCSK_KEX2_1 | 405 | 407 | PF00082 | 0.415 |
CLV_PCSK_KEX2_1 | 98 | 100 | PF00082 | 0.618 |
CLV_PCSK_SKI1_1 | 180 | 184 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 224 | 228 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 339 | 343 | PF00082 | 0.382 |
CLV_Separin_Metazoa | 365 | 369 | PF03568 | 0.405 |
DEG_APCC_DBOX_1 | 196 | 204 | PF00400 | 0.460 |
DOC_CKS1_1 | 68 | 73 | PF01111 | 0.578 |
DOC_CKS1_1 | 85 | 90 | PF01111 | 0.530 |
DOC_MAPK_gen_1 | 246 | 254 | PF00069 | 0.470 |
DOC_MAPK_gen_1 | 388 | 395 | PF00069 | 0.566 |
DOC_MAPK_MEF2A_6 | 192 | 200 | PF00069 | 0.432 |
DOC_MAPK_MEF2A_6 | 248 | 256 | PF00069 | 0.426 |
DOC_PP1_RVXF_1 | 366 | 372 | PF00149 | 0.409 |
DOC_PP2B_LxvP_1 | 256 | 259 | PF13499 | 0.450 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.627 |
DOC_USP7_MATH_1 | 122 | 126 | PF00917 | 0.450 |
DOC_USP7_MATH_1 | 141 | 145 | PF00917 | 0.480 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.378 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.560 |
DOC_USP7_MATH_1 | 210 | 214 | PF00917 | 0.471 |
DOC_USP7_MATH_1 | 240 | 244 | PF00917 | 0.475 |
DOC_USP7_MATH_1 | 321 | 325 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 348 | 352 | PF00917 | 0.425 |
DOC_USP7_MATH_1 | 386 | 390 | PF00917 | 0.465 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.717 |
DOC_WW_Pin1_4 | 113 | 118 | PF00397 | 0.730 |
DOC_WW_Pin1_4 | 170 | 175 | PF00397 | 0.621 |
DOC_WW_Pin1_4 | 271 | 276 | PF00397 | 0.679 |
DOC_WW_Pin1_4 | 67 | 72 | PF00397 | 0.557 |
DOC_WW_Pin1_4 | 84 | 89 | PF00397 | 0.772 |
DOC_WW_Pin1_4 | 9 | 14 | PF00397 | 0.545 |
LIG_14-3-3_CanoR_1 | 197 | 201 | PF00244 | 0.531 |
LIG_14-3-3_CanoR_1 | 268 | 277 | PF00244 | 0.561 |
LIG_14-3-3_CanoR_1 | 320 | 326 | PF00244 | 0.560 |
LIG_14-3-3_CanoR_1 | 394 | 401 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 410 | 417 | PF00244 | 0.432 |
LIG_Actin_WH2_2 | 187 | 203 | PF00022 | 0.435 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.540 |
LIG_BRCT_BRCA1_1 | 29 | 33 | PF00533 | 0.531 |
LIG_Clathr_ClatBox_1 | 157 | 161 | PF01394 | 0.457 |
LIG_FHA_1 | 144 | 150 | PF00498 | 0.548 |
LIG_FHA_1 | 227 | 233 | PF00498 | 0.384 |
LIG_FHA_1 | 358 | 364 | PF00498 | 0.333 |
LIG_FHA_1 | 37 | 43 | PF00498 | 0.490 |
LIG_FHA_2 | 167 | 173 | PF00498 | 0.557 |
LIG_FHA_2 | 183 | 189 | PF00498 | 0.307 |
LIG_FHA_2 | 373 | 379 | PF00498 | 0.564 |
LIG_FHA_2 | 382 | 388 | PF00498 | 0.515 |
LIG_FHA_2 | 68 | 74 | PF00498 | 0.542 |
LIG_HP1_1 | 196 | 200 | PF01393 | 0.440 |
LIG_LIR_Apic_2 | 12 | 17 | PF02991 | 0.544 |
LIG_LIR_Gen_1 | 181 | 190 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 181 | 186 | PF02991 | 0.458 |
LIG_SH2_PTP2 | 14 | 17 | PF00017 | 0.594 |
LIG_SH2_SRC | 14 | 17 | PF00017 | 0.599 |
LIG_SH2_STAT3 | 231 | 234 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 14 | 17 | PF00017 | 0.678 |
LIG_SH2_STAT5 | 231 | 234 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 38 | 41 | PF00017 | 0.441 |
LIG_SH3_1 | 10 | 16 | PF00018 | 0.542 |
LIG_SH3_1 | 168 | 174 | PF00018 | 0.585 |
LIG_SH3_3 | 10 | 16 | PF00018 | 0.616 |
LIG_SH3_3 | 168 | 174 | PF00018 | 0.627 |
LIG_SH3_3 | 230 | 236 | PF00018 | 0.384 |
LIG_SH3_3 | 82 | 88 | PF00018 | 0.675 |
LIG_SH3_3 | 91 | 97 | PF00018 | 0.662 |
LIG_SUMO_SIM_anti_2 | 249 | 255 | PF11976 | 0.422 |
LIG_SUMO_SIM_par_1 | 156 | 161 | PF11976 | 0.450 |
LIG_SUMO_SIM_par_1 | 249 | 255 | PF11976 | 0.403 |
LIG_SUMO_SIM_par_1 | 351 | 358 | PF11976 | 0.400 |
LIG_TRAF2_1 | 112 | 115 | PF00917 | 0.597 |
LIG_TRAF2_1 | 61 | 64 | PF00917 | 0.527 |
LIG_WRC_WIRS_1 | 4 | 9 | PF05994 | 0.527 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.450 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.517 |
MOD_CK1_1 | 269 | 275 | PF00069 | 0.613 |
MOD_CK1_1 | 276 | 282 | PF00069 | 0.523 |
MOD_CK1_1 | 355 | 361 | PF00069 | 0.492 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.480 |
MOD_CK1_1 | 389 | 395 | PF00069 | 0.606 |
MOD_CK2_1 | 2 | 8 | PF00069 | 0.593 |
MOD_CK2_1 | 372 | 378 | PF00069 | 0.549 |
MOD_CK2_1 | 381 | 387 | PF00069 | 0.516 |
MOD_CK2_1 | 67 | 73 | PF00069 | 0.567 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.475 |
MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.424 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.480 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.726 |
MOD_GlcNHglycan | 412 | 415 | PF01048 | 0.536 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.651 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.595 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.552 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.577 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.434 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.452 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.572 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.360 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.607 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.496 |
MOD_NEK2_1 | 160 | 165 | PF00069 | 0.483 |
MOD_NEK2_1 | 182 | 187 | PF00069 | 0.579 |
MOD_NEK2_1 | 227 | 232 | PF00069 | 0.361 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.425 |
MOD_NEK2_1 | 263 | 268 | PF00069 | 0.419 |
MOD_NEK2_1 | 33 | 38 | PF00069 | 0.424 |
MOD_NEK2_1 | 342 | 347 | PF00069 | 0.371 |
MOD_NEK2_1 | 393 | 398 | PF00069 | 0.543 |
MOD_NEK2_2 | 196 | 201 | PF00069 | 0.454 |
MOD_OFUCOSY | 35 | 40 | PF10250 | 0.463 |
MOD_PIKK_1 | 303 | 309 | PF00454 | 0.357 |
MOD_PIKK_1 | 348 | 354 | PF00454 | 0.424 |
MOD_PIKK_1 | 393 | 399 | PF00454 | 0.497 |
MOD_PK_1 | 246 | 252 | PF00069 | 0.425 |
MOD_PKA_2 | 196 | 202 | PF00069 | 0.532 |
MOD_PKA_2 | 270 | 276 | PF00069 | 0.591 |
MOD_PKA_2 | 319 | 325 | PF00069 | 0.551 |
MOD_PKA_2 | 389 | 395 | PF00069 | 0.564 |
MOD_PKA_2 | 64 | 70 | PF00069 | 0.592 |
MOD_Plk_1 | 254 | 260 | PF00069 | 0.406 |
MOD_Plk_4 | 160 | 166 | PF00069 | 0.524 |
MOD_Plk_4 | 227 | 233 | PF00069 | 0.384 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.714 |
MOD_ProDKin_1 | 170 | 176 | PF00069 | 0.618 |
MOD_ProDKin_1 | 271 | 277 | PF00069 | 0.680 |
MOD_ProDKin_1 | 67 | 73 | PF00069 | 0.565 |
MOD_ProDKin_1 | 84 | 90 | PF00069 | 0.772 |
MOD_ProDKin_1 | 9 | 15 | PF00069 | 0.549 |
MOD_SUMO_for_1 | 281 | 284 | PF00179 | 0.500 |
MOD_SUMO_rev_2 | 274 | 283 | PF00179 | 0.589 |
TRG_DiLeu_BaEn_1 | 365 | 370 | PF01217 | 0.402 |
TRG_DiLeu_BaEn_4 | 63 | 69 | PF01217 | 0.521 |
TRG_DiLeu_BaLyEn_6 | 198 | 203 | PF01217 | 0.453 |
TRG_DiLeu_LyEn_5 | 365 | 370 | PF01217 | 0.402 |
TRG_ER_diArg_1 | 285 | 288 | PF00400 | 0.475 |
TRG_ER_diArg_1 | 405 | 407 | PF00400 | 0.415 |
TRG_ER_diArg_1 | 97 | 99 | PF00400 | 0.624 |
TRG_Pf-PMV_PEXEL_1 | 180 | 184 | PF00026 | 0.445 |
TRG_Pf-PMV_PEXEL_1 | 287 | 292 | PF00026 | 0.435 |
TRG_Pf-PMV_PEXEL_1 | 405 | 409 | PF00026 | 0.408 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDW8 | Leptomonas seymouri | 37% | 72% |
A0A3S7X7D6 | Leishmania donovani | 91% | 100% |
A4HAF6 | Leishmania braziliensis | 71% | 100% |
A4I9L2 | Leishmania infantum | 91% | 100% |
E9B4L0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |