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: Q4QCA7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 332 | 336 | PF00656 | 0.571 |
CLV_C14_Caspase3-7 | 386 | 390 | PF00656 | 0.480 |
CLV_C14_Caspase3-7 | 404 | 408 | PF00656 | 0.636 |
CLV_C14_Caspase3-7 | 92 | 96 | PF00656 | 0.626 |
CLV_NRD_NRD_1 | 133 | 135 | PF00675 | 0.733 |
CLV_NRD_NRD_1 | 200 | 202 | PF00675 | 0.709 |
CLV_NRD_NRD_1 | 251 | 253 | PF00675 | 0.576 |
CLV_NRD_NRD_1 | 275 | 277 | PF00675 | 0.699 |
CLV_NRD_NRD_1 | 340 | 342 | PF00675 | 0.625 |
CLV_NRD_NRD_1 | 344 | 346 | PF00675 | 0.588 |
CLV_NRD_NRD_1 | 368 | 370 | PF00675 | 0.513 |
CLV_PCSK_KEX2_1 | 133 | 135 | PF00082 | 0.733 |
CLV_PCSK_KEX2_1 | 199 | 201 | PF00082 | 0.729 |
CLV_PCSK_KEX2_1 | 251 | 253 | PF00082 | 0.576 |
CLV_PCSK_KEX2_1 | 275 | 277 | PF00082 | 0.696 |
CLV_PCSK_KEX2_1 | 340 | 342 | PF00082 | 0.631 |
CLV_PCSK_SKI1_1 | 11 | 15 | PF00082 | 0.569 |
CLV_PCSK_SKI1_1 | 194 | 198 | PF00082 | 0.589 |
CLV_PCSK_SKI1_1 | 306 | 310 | PF00082 | 0.600 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.535 |
DEG_SCF_FBW7_1 | 100 | 105 | PF00400 | 0.647 |
DEG_SPOP_SBC_1 | 102 | 106 | PF00917 | 0.636 |
DEG_SPOP_SBC_1 | 189 | 193 | PF00917 | 0.608 |
DEG_SPOP_SBC_1 | 318 | 322 | PF00917 | 0.692 |
DOC_MAPK_gen_1 | 251 | 257 | PF00069 | 0.484 |
DOC_MAPK_gen_1 | 275 | 282 | PF00069 | 0.625 |
DOC_MAPK_HePTP_8 | 197 | 214 | PF00069 | 0.441 |
DOC_MAPK_MEF2A_6 | 110 | 118 | PF00069 | 0.518 |
DOC_MAPK_MEF2A_6 | 275 | 284 | PF00069 | 0.615 |
DOC_PP2B_LxvP_1 | 36 | 39 | PF13499 | 0.636 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.681 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.576 |
DOC_USP7_MATH_1 | 317 | 321 | PF00917 | 0.715 |
DOC_USP7_MATH_1 | 325 | 329 | PF00917 | 0.609 |
DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.649 |
LIG_14-3-3_CanoR_1 | 11 | 16 | PF00244 | 0.595 |
LIG_14-3-3_CanoR_1 | 110 | 114 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 275 | 282 | PF00244 | 0.625 |
LIG_14-3-3_CanoR_1 | 369 | 373 | PF00244 | 0.535 |
LIG_Actin_WH2_2 | 72 | 88 | PF00022 | 0.675 |
LIG_BRCT_BRCA1_1 | 28 | 32 | PF00533 | 0.426 |
LIG_FHA_1 | 103 | 109 | PF00498 | 0.686 |
LIG_FHA_1 | 110 | 116 | PF00498 | 0.477 |
LIG_FHA_1 | 17 | 23 | PF00498 | 0.446 |
LIG_FHA_1 | 191 | 197 | PF00498 | 0.664 |
LIG_FHA_1 | 217 | 223 | PF00498 | 0.573 |
LIG_FHA_1 | 248 | 254 | PF00498 | 0.381 |
LIG_FHA_1 | 355 | 361 | PF00498 | 0.465 |
LIG_FHA_1 | 80 | 86 | PF00498 | 0.471 |
LIG_FHA_2 | 175 | 181 | PF00498 | 0.751 |
LIG_FHA_2 | 201 | 207 | PF00498 | 0.472 |
LIG_FHA_2 | 231 | 237 | PF00498 | 0.481 |
LIG_FHA_2 | 442 | 448 | PF00498 | 0.638 |
LIG_LIR_Gen_1 | 112 | 120 | PF02991 | 0.430 |
LIG_LIR_Gen_1 | 29 | 39 | PF02991 | 0.469 |
LIG_LIR_Gen_1 | 350 | 360 | PF02991 | 0.471 |
LIG_LIR_Gen_1 | 430 | 439 | PF02991 | 0.506 |
LIG_LIR_Gen_1 | 59 | 66 | PF02991 | 0.575 |
LIG_LIR_Nem_3 | 112 | 116 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 29 | 35 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 350 | 355 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 430 | 434 | PF02991 | 0.550 |
LIG_LIR_Nem_3 | 59 | 64 | PF02991 | 0.566 |
LIG_SH2_PTP2 | 113 | 116 | PF00017 | 0.506 |
LIG_SH2_SRC | 148 | 151 | PF00017 | 0.441 |
LIG_SH2_SRC | 387 | 390 | PF00017 | 0.480 |
LIG_SH2_STAP1 | 356 | 360 | PF00017 | 0.441 |
LIG_SH2_STAP1 | 421 | 425 | PF00017 | 0.680 |
LIG_SH2_STAT5 | 113 | 116 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 148 | 151 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 356 | 359 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 387 | 390 | PF00017 | 0.480 |
LIG_SH3_3 | 10 | 16 | PF00018 | 0.549 |
LIG_SH3_3 | 257 | 263 | PF00018 | 0.690 |
LIG_SH3_3 | 411 | 417 | PF00018 | 0.639 |
LIG_SUMO_SIM_anti_2 | 112 | 119 | PF11976 | 0.501 |
LIG_SUMO_SIM_anti_2 | 211 | 216 | PF11976 | 0.388 |
LIG_SUMO_SIM_par_1 | 112 | 119 | PF11976 | 0.447 |
LIG_SUMO_SIM_par_1 | 218 | 223 | PF11976 | 0.564 |
LIG_SUMO_SIM_par_1 | 280 | 285 | PF11976 | 0.582 |
LIG_UBA3_1 | 299 | 306 | PF00899 | 0.556 |
LIG_WRC_WIRS_1 | 363 | 368 | PF05994 | 0.605 |
LIG_WW_3 | 64 | 68 | PF00397 | 0.517 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.585 |
MOD_CK1_1 | 128 | 134 | PF00069 | 0.467 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.729 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.594 |
MOD_CK1_1 | 190 | 196 | PF00069 | 0.554 |
MOD_CK1_1 | 358 | 364 | PF00069 | 0.478 |
MOD_CK1_1 | 89 | 95 | PF00069 | 0.572 |
MOD_CK2_1 | 230 | 236 | PF00069 | 0.489 |
MOD_CK2_1 | 362 | 368 | PF00069 | 0.501 |
MOD_CK2_1 | 441 | 447 | PF00069 | 0.626 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.668 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.599 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.449 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.659 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.620 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.691 |
MOD_GlcNHglycan | 241 | 244 | PF01048 | 0.383 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.457 |
MOD_GlcNHglycan | 270 | 273 | PF01048 | 0.685 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.753 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.552 |
MOD_GlcNHglycan | 393 | 396 | PF01048 | 0.734 |
MOD_GlcNHglycan | 400 | 404 | PF01048 | 0.657 |
MOD_GlcNHglycan | 435 | 438 | PF01048 | 0.567 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.590 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.565 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.733 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.549 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.628 |
MOD_GSK3_1 | 313 | 320 | PF00069 | 0.604 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.617 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.466 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.531 |
MOD_GSK3_1 | 373 | 380 | PF00069 | 0.550 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.484 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.676 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.569 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.666 |
MOD_N-GLC_1 | 181 | 186 | PF02516 | 0.706 |
MOD_N-GLC_1 | 216 | 221 | PF02516 | 0.499 |
MOD_N-GLC_1 | 225 | 230 | PF02516 | 0.567 |
MOD_N-GLC_2 | 268 | 270 | PF02516 | 0.629 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.567 |
MOD_NEK2_1 | 286 | 291 | PF00069 | 0.463 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.591 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.443 |
MOD_NEK2_1 | 87 | 92 | PF00069 | 0.475 |
MOD_NEK2_2 | 16 | 21 | PF00069 | 0.469 |
MOD_NEK2_2 | 319 | 324 | PF00069 | 0.657 |
MOD_NEK2_2 | 56 | 61 | PF00069 | 0.621 |
MOD_PIKK_1 | 340 | 346 | PF00454 | 0.605 |
MOD_PIKK_1 | 65 | 71 | PF00454 | 0.474 |
MOD_PIKK_1 | 77 | 83 | PF00454 | 0.571 |
MOD_PKA_1 | 200 | 206 | PF00069 | 0.551 |
MOD_PKA_1 | 340 | 346 | PF00069 | 0.623 |
MOD_PKA_2 | 109 | 115 | PF00069 | 0.574 |
MOD_PKA_2 | 200 | 206 | PF00069 | 0.591 |
MOD_PKA_2 | 274 | 280 | PF00069 | 0.679 |
MOD_PKA_2 | 340 | 346 | PF00069 | 0.650 |
MOD_PKA_2 | 368 | 374 | PF00069 | 0.466 |
MOD_Plk_1 | 216 | 222 | PF00069 | 0.529 |
MOD_Plk_1 | 26 | 32 | PF00069 | 0.422 |
MOD_Plk_1 | 329 | 335 | PF00069 | 0.592 |
MOD_Plk_1 | 361 | 367 | PF00069 | 0.468 |
MOD_Plk_2-3 | 362 | 368 | PF00069 | 0.496 |
MOD_Plk_4 | 109 | 115 | PF00069 | 0.544 |
MOD_Plk_4 | 208 | 214 | PF00069 | 0.386 |
MOD_Plk_4 | 319 | 325 | PF00069 | 0.686 |
MOD_Plk_4 | 355 | 361 | PF00069 | 0.448 |
MOD_Plk_4 | 56 | 62 | PF00069 | 0.627 |
MOD_Plk_4 | 79 | 85 | PF00069 | 0.478 |
MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.649 |
MOD_SUMO_rev_2 | 362 | 372 | PF00179 | 0.491 |
TRG_DiLeu_BaLyEn_6 | 31 | 36 | PF01217 | 0.403 |
TRG_ENDOCYTIC_2 | 113 | 116 | PF00928 | 0.426 |
TRG_ENDOCYTIC_2 | 356 | 359 | PF00928 | 0.444 |
TRG_ER_diArg_1 | 199 | 201 | PF00400 | 0.726 |
TRG_ER_diArg_1 | 251 | 253 | PF00400 | 0.485 |
TRG_ER_diArg_1 | 339 | 341 | PF00400 | 0.628 |
TRG_Pf-PMV_PEXEL_1 | 252 | 256 | PF00026 | 0.517 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ILY1 | Leptomonas seymouri | 48% | 100% |
A0A3S7WWI8 | Leishmania donovani | 91% | 100% |
A4HK96 | Leishmania braziliensis | 70% | 100% |
E9AGV8 | Leishmania infantum | 91% | 100% |
E9AV74 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |