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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: Q4Q8M8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 88 | 92 | PF00656 | 0.486 |
CLV_PCSK_KEX2_1 | 115 | 117 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 70 | 72 | PF00082 | 0.471 |
CLV_PCSK_PC1ET2_1 | 115 | 117 | PF00082 | 0.494 |
CLV_PCSK_PC1ET2_1 | 70 | 72 | PF00082 | 0.471 |
CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.465 |
CLV_PCSK_SKI1_1 | 281 | 285 | PF00082 | 0.415 |
CLV_PCSK_SKI1_1 | 327 | 331 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 372 | 376 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 389 | 393 | PF00082 | 0.321 |
CLV_PCSK_SKI1_1 | 39 | 43 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 8 | 12 | PF00082 | 0.473 |
DEG_APCC_DBOX_1 | 106 | 114 | PF00400 | 0.303 |
DEG_SCF_FBW7_1 | 254 | 259 | PF00400 | 0.643 |
DOC_CKS1_1 | 185 | 190 | PF01111 | 0.491 |
DOC_MAPK_gen_1 | 276 | 285 | PF00069 | 0.557 |
DOC_MAPK_gen_1 | 380 | 388 | PF00069 | 0.552 |
DOC_MAPK_gen_1 | 8 | 18 | PF00069 | 0.463 |
DOC_MAPK_MEF2A_6 | 313 | 320 | PF00069 | 0.511 |
DOC_USP7_MATH_1 | 249 | 253 | PF00917 | 0.588 |
DOC_USP7_MATH_1 | 264 | 268 | PF00917 | 0.665 |
DOC_USP7_MATH_1 | 297 | 301 | PF00917 | 0.475 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.484 |
DOC_USP7_MATH_1 | 358 | 362 | PF00917 | 0.475 |
DOC_USP7_UBL2_3 | 406 | 410 | PF12436 | 0.562 |
DOC_USP7_UBL2_3 | 66 | 70 | PF12436 | 0.466 |
DOC_WW_Pin1_4 | 184 | 189 | PF00397 | 0.488 |
DOC_WW_Pin1_4 | 252 | 257 | PF00397 | 0.744 |
LIG_14-3-3_CanoR_1 | 231 | 239 | PF00244 | 0.629 |
LIG_14-3-3_CanoR_1 | 240 | 248 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 281 | 286 | PF00244 | 0.563 |
LIG_14-3-3_CanoR_1 | 350 | 354 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 382 | 387 | PF00244 | 0.334 |
LIG_14-3-3_CanoR_1 | 82 | 87 | PF00244 | 0.492 |
LIG_APCC_ABBA_1 | 22 | 27 | PF00400 | 0.338 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.558 |
LIG_BRCT_BRCA1_1 | 384 | 388 | PF00533 | 0.472 |
LIG_BRCT_BRCA1_1 | 54 | 58 | PF00533 | 0.523 |
LIG_FHA_1 | 101 | 107 | PF00498 | 0.437 |
LIG_FHA_1 | 205 | 211 | PF00498 | 0.469 |
LIG_FHA_1 | 219 | 225 | PF00498 | 0.310 |
LIG_FHA_1 | 253 | 259 | PF00498 | 0.744 |
LIG_FHA_1 | 307 | 313 | PF00498 | 0.341 |
LIG_FHA_1 | 366 | 372 | PF00498 | 0.510 |
LIG_FHA_1 | 63 | 69 | PF00498 | 0.404 |
LIG_FHA_2 | 185 | 191 | PF00498 | 0.542 |
LIG_FHA_2 | 240 | 246 | PF00498 | 0.760 |
LIG_FHA_2 | 410 | 416 | PF00498 | 0.309 |
LIG_LIR_Apic_2 | 184 | 188 | PF02991 | 0.484 |
LIG_LIR_Gen_1 | 325 | 332 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 334 | 343 | PF02991 | 0.307 |
LIG_LIR_Gen_1 | 83 | 91 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 325 | 331 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 334 | 340 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 385 | 391 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 55 | 61 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 83 | 89 | PF02991 | 0.449 |
LIG_SH2_CRK | 185 | 189 | PF00017 | 0.490 |
LIG_SH2_NCK_1 | 185 | 189 | PF00017 | 0.565 |
LIG_SH2_STAP1 | 195 | 199 | PF00017 | 0.496 |
LIG_SH2_STAP1 | 308 | 312 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 185 | 188 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 25 | 28 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 308 | 311 | PF00017 | 0.487 |
LIG_SH3_3 | 221 | 227 | PF00018 | 0.450 |
LIG_SH3_4 | 410 | 417 | PF00018 | 0.461 |
LIG_SH3_4 | 50 | 57 | PF00018 | 0.493 |
LIG_SUMO_SIM_anti_2 | 20 | 25 | PF11976 | 0.257 |
LIG_TYR_ITIM | 23 | 28 | PF00017 | 0.253 |
LIG_UBA3_1 | 398 | 406 | PF00899 | 0.378 |
MOD_CK1_1 | 120 | 126 | PF00069 | 0.441 |
MOD_CK1_1 | 184 | 190 | PF00069 | 0.571 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.673 |
MOD_CK1_1 | 300 | 306 | PF00069 | 0.671 |
MOD_CK1_1 | 37 | 43 | PF00069 | 0.438 |
MOD_CK1_1 | 384 | 390 | PF00069 | 0.400 |
MOD_CK1_1 | 402 | 408 | PF00069 | 0.357 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.430 |
MOD_CK2_1 | 184 | 190 | PF00069 | 0.496 |
MOD_CK2_1 | 358 | 364 | PF00069 | 0.469 |
MOD_CK2_1 | 384 | 390 | PF00069 | 0.481 |
MOD_CK2_1 | 409 | 415 | PF00069 | 0.312 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.514 |
MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.753 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.673 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.653 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.672 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.451 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.462 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.429 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.491 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.744 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.442 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.504 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.541 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.360 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.350 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.454 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.493 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.428 |
MOD_N-GLC_1 | 264 | 269 | PF02516 | 0.696 |
MOD_N-GLC_1 | 281 | 286 | PF02516 | 0.491 |
MOD_NEK2_1 | 117 | 122 | PF00069 | 0.532 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.359 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.584 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.550 |
MOD_NEK2_1 | 191 | 196 | PF00069 | 0.515 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.398 |
MOD_NEK2_1 | 320 | 325 | PF00069 | 0.469 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.422 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.394 |
MOD_NEK2_1 | 81 | 86 | PF00069 | 0.471 |
MOD_NEK2_2 | 349 | 354 | PF00069 | 0.443 |
MOD_PIKK_1 | 171 | 177 | PF00454 | 0.537 |
MOD_PIKK_1 | 256 | 262 | PF00454 | 0.701 |
MOD_PIKK_1 | 300 | 306 | PF00454 | 0.563 |
MOD_PKA_2 | 239 | 245 | PF00069 | 0.696 |
MOD_PKA_2 | 349 | 355 | PF00069 | 0.534 |
MOD_PKA_2 | 381 | 387 | PF00069 | 0.339 |
MOD_PKA_2 | 81 | 87 | PF00069 | 0.485 |
MOD_Plk_1 | 234 | 240 | PF00069 | 0.751 |
MOD_Plk_1 | 281 | 287 | PF00069 | 0.453 |
MOD_Plk_4 | 120 | 126 | PF00069 | 0.406 |
MOD_Plk_4 | 17 | 23 | PF00069 | 0.469 |
MOD_Plk_4 | 218 | 224 | PF00069 | 0.394 |
MOD_Plk_4 | 37 | 43 | PF00069 | 0.425 |
MOD_Plk_4 | 394 | 400 | PF00069 | 0.550 |
MOD_ProDKin_1 | 184 | 190 | PF00069 | 0.484 |
MOD_ProDKin_1 | 252 | 258 | PF00069 | 0.742 |
MOD_SUMO_rev_2 | 2 | 10 | PF00179 | 0.592 |
MOD_SUMO_rev_2 | 243 | 249 | PF00179 | 0.767 |
MOD_SUMO_rev_2 | 271 | 280 | PF00179 | 0.637 |
TRG_ENDOCYTIC_2 | 147 | 150 | PF00928 | 0.413 |
TRG_ENDOCYTIC_2 | 25 | 28 | PF00928 | 0.364 |
TRG_NES_CRM1_1 | 390 | 403 | PF08389 | 0.467 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IJS3 | Leptomonas seymouri | 54% | 100% |
A0A0S4KFQ7 | Bodo saltans | 28% | 100% |
A0A1X0NYM7 | Trypanosomatidae | 30% | 87% |
A0A3R7KQG6 | Trypanosoma rangeli | 39% | 95% |
A0A3S7X164 | Leishmania donovani | 91% | 100% |
A4I3A5 | Leishmania infantum | 91% | 100% |
D0A828 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
E9AZK3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
V5B0U4 | Trypanosoma cruzi | 34% | 90% |