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: Q4QHI3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 108 | 112 | PF00656 | 0.654 |
CLV_C14_Caspase3-7 | 203 | 207 | PF00656 | 0.628 |
CLV_C14_Caspase3-7 | 263 | 267 | PF00656 | 0.607 |
CLV_NRD_NRD_1 | 252 | 254 | PF00675 | 0.444 |
CLV_PCSK_FUR_1 | 418 | 422 | PF00082 | 0.652 |
CLV_PCSK_KEX2_1 | 252 | 254 | PF00082 | 0.444 |
CLV_PCSK_KEX2_1 | 420 | 422 | PF00082 | 0.605 |
CLV_PCSK_PC1ET2_1 | 420 | 422 | PF00082 | 0.677 |
CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.664 |
CLV_PCSK_SKI1_1 | 167 | 171 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 22 | 26 | PF00082 | 0.536 |
CLV_Separin_Metazoa | 320 | 324 | PF03568 | 0.496 |
DEG_APCC_DBOX_1 | 73 | 81 | PF00400 | 0.536 |
DEG_SPOP_SBC_1 | 10 | 14 | PF00917 | 0.587 |
DOC_MAPK_FxFP_2 | 32 | 35 | PF00069 | 0.373 |
DOC_MAPK_MEF2A_6 | 295 | 304 | PF00069 | 0.537 |
DOC_PP2B_LxvP_1 | 197 | 200 | PF13499 | 0.448 |
DOC_PP4_FxxP_1 | 32 | 35 | PF00568 | 0.464 |
DOC_USP7_MATH_1 | 390 | 394 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 406 | 410 | PF00917 | 0.553 |
DOC_WW_Pin1_4 | 183 | 188 | PF00397 | 0.622 |
DOC_WW_Pin1_4 | 205 | 210 | PF00397 | 0.612 |
DOC_WW_Pin1_4 | 307 | 312 | PF00397 | 0.596 |
DOC_WW_Pin1_4 | 394 | 399 | PF00397 | 0.608 |
LIG_14-3-3_CanoR_1 | 147 | 153 | PF00244 | 0.488 |
LIG_14-3-3_CanoR_1 | 22 | 32 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 252 | 260 | PF00244 | 0.513 |
LIG_14-3-3_CanoR_1 | 323 | 333 | PF00244 | 0.490 |
LIG_14-3-3_CanoR_1 | 37 | 46 | PF00244 | 0.467 |
LIG_14-3-3_CanoR_1 | 97 | 104 | PF00244 | 0.504 |
LIG_Actin_WH2_2 | 131 | 149 | PF00022 | 0.522 |
LIG_Actin_WH2_2 | 315 | 332 | PF00022 | 0.574 |
LIG_BIR_III_2 | 206 | 210 | PF00653 | 0.578 |
LIG_BRCT_BRCA1_1 | 30 | 34 | PF00533 | 0.396 |
LIG_FHA_1 | 147 | 153 | PF00498 | 0.501 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.415 |
LIG_FHA_1 | 208 | 214 | PF00498 | 0.694 |
LIG_FHA_1 | 23 | 29 | PF00498 | 0.467 |
LIG_FHA_1 | 39 | 45 | PF00498 | 0.565 |
LIG_FHA_2 | 201 | 207 | PF00498 | 0.543 |
LIG_FHA_2 | 312 | 318 | PF00498 | 0.589 |
LIG_GBD_Chelix_1 | 290 | 298 | PF00786 | 0.523 |
LIG_LIR_Apic_2 | 31 | 35 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 157 | 165 | PF02991 | 0.419 |
LIG_LIR_Gen_1 | 219 | 230 | PF02991 | 0.626 |
LIG_LIR_Nem_3 | 157 | 162 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 219 | 225 | PF02991 | 0.517 |
LIG_PDZ_Wminus1_1 | 432 | 434 | PF00595 | 0.539 |
LIG_SH2_SRC | 198 | 201 | PF00017 | 0.463 |
LIG_SH2_STAP1 | 165 | 169 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 198 | 201 | PF00017 | 0.625 |
LIG_SH2_STAT5 | 259 | 262 | PF00017 | 0.580 |
LIG_SH2_STAT5 | 90 | 93 | PF00017 | 0.424 |
LIG_SH3_3 | 178 | 184 | PF00018 | 0.704 |
LIG_SH3_3 | 331 | 337 | PF00018 | 0.588 |
LIG_SH3_3 | 338 | 344 | PF00018 | 0.663 |
LIG_SH3_3 | 400 | 406 | PF00018 | 0.653 |
LIG_SUMO_SIM_anti_2 | 317 | 324 | PF11976 | 0.663 |
LIG_SUMO_SIM_par_1 | 160 | 166 | PF11976 | 0.401 |
LIG_SUMO_SIM_par_1 | 357 | 363 | PF11976 | 0.484 |
LIG_TRAF2_1 | 209 | 212 | PF00917 | 0.618 |
LIG_TRAF2_1 | 286 | 289 | PF00917 | 0.551 |
LIG_TRAF2_1 | 351 | 354 | PF00917 | 0.582 |
LIG_WW_2 | 405 | 408 | PF00397 | 0.550 |
MOD_CDK_SPK_2 | 394 | 399 | PF00069 | 0.676 |
MOD_CK1_1 | 113 | 119 | PF00069 | 0.491 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.520 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.463 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.516 |
MOD_CK1_1 | 237 | 243 | PF00069 | 0.582 |
MOD_CK1_1 | 307 | 313 | PF00069 | 0.676 |
MOD_CK1_1 | 335 | 341 | PF00069 | 0.679 |
MOD_CK1_1 | 383 | 389 | PF00069 | 0.566 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.620 |
MOD_CK2_1 | 205 | 211 | PF00069 | 0.549 |
MOD_CK2_1 | 215 | 221 | PF00069 | 0.451 |
MOD_CK2_1 | 411 | 417 | PF00069 | 0.657 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.650 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.613 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.735 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.406 |
MOD_GlcNHglycan | 356 | 359 | PF01048 | 0.525 |
MOD_GlcNHglycan | 385 | 388 | PF01048 | 0.536 |
MOD_GlcNHglycan | 408 | 411 | PF01048 | 0.588 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.684 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.619 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.604 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.497 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.472 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.670 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.593 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.465 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.709 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.578 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.586 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.559 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.724 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.679 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.611 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.516 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.517 |
MOD_LATS_1 | 369 | 375 | PF00433 | 0.509 |
MOD_N-GLC_1 | 226 | 231 | PF02516 | 0.511 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.611 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.490 |
MOD_NEK2_1 | 278 | 283 | PF00069 | 0.576 |
MOD_NEK2_1 | 290 | 295 | PF00069 | 0.404 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.556 |
MOD_NEK2_1 | 321 | 326 | PF00069 | 0.672 |
MOD_NEK2_1 | 380 | 385 | PF00069 | 0.607 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.535 |
MOD_PIKK_1 | 110 | 116 | PF00454 | 0.553 |
MOD_PIKK_1 | 270 | 276 | PF00454 | 0.606 |
MOD_PIKK_1 | 278 | 284 | PF00454 | 0.479 |
MOD_PIKK_1 | 335 | 341 | PF00454 | 0.633 |
MOD_PK_1 | 147 | 153 | PF00069 | 0.464 |
MOD_PKA_2 | 146 | 152 | PF00069 | 0.487 |
MOD_PKA_2 | 4 | 10 | PF00069 | 0.460 |
MOD_PKA_2 | 96 | 102 | PF00069 | 0.620 |
MOD_Plk_1 | 211 | 217 | PF00069 | 0.536 |
MOD_Plk_1 | 226 | 232 | PF00069 | 0.465 |
MOD_Plk_1 | 52 | 58 | PF00069 | 0.466 |
MOD_Plk_2-3 | 349 | 355 | PF00069 | 0.496 |
MOD_Plk_4 | 147 | 153 | PF00069 | 0.515 |
MOD_Plk_4 | 226 | 232 | PF00069 | 0.515 |
MOD_Plk_4 | 52 | 58 | PF00069 | 0.483 |
MOD_ProDKin_1 | 183 | 189 | PF00069 | 0.616 |
MOD_ProDKin_1 | 205 | 211 | PF00069 | 0.612 |
MOD_ProDKin_1 | 307 | 313 | PF00069 | 0.597 |
MOD_ProDKin_1 | 394 | 400 | PF00069 | 0.609 |
MOD_SUMO_for_1 | 124 | 127 | PF00179 | 0.656 |
TRG_DiLeu_BaLyEn_6 | 292 | 297 | PF01217 | 0.451 |
TRG_ER_diArg_1 | 251 | 253 | PF00400 | 0.449 |
TRG_NES_CRM1_1 | 288 | 303 | PF08389 | 0.485 |
TRG_NES_CRM1_1 | 353 | 365 | PF08389 | 0.565 |
TRG_NLS_MonoExtC_3 | 121 | 127 | PF00514 | 0.592 |
TRG_Pf-PMV_PEXEL_1 | 299 | 303 | PF00026 | 0.488 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYC0 | Leptomonas seymouri | 35% | 80% |
A0A3Q8I7N0 | Leishmania donovani | 91% | 100% |
A4H616 | Leishmania braziliensis | 68% | 92% |
A4HUE3 | Leishmania infantum | 91% | 100% |
E9AN43 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |