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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 1, no: 9 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A4HIX3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 132 | 134 | PF00675 | 0.472 |
CLV_NRD_NRD_1 | 168 | 170 | PF00675 | 0.399 |
CLV_NRD_NRD_1 | 177 | 179 | PF00675 | 0.467 |
CLV_NRD_NRD_1 | 312 | 314 | PF00675 | 0.638 |
CLV_NRD_NRD_1 | 70 | 72 | PF00675 | 0.465 |
CLV_PCSK_KEX2_1 | 168 | 170 | PF00082 | 0.400 |
CLV_PCSK_KEX2_1 | 179 | 181 | PF00082 | 0.443 |
CLV_PCSK_KEX2_1 | 31 | 33 | PF00082 | 0.448 |
CLV_PCSK_KEX2_1 | 311 | 313 | PF00082 | 0.684 |
CLV_PCSK_PC1ET2_1 | 179 | 181 | PF00082 | 0.484 |
CLV_PCSK_PC1ET2_1 | 31 | 33 | PF00082 | 0.448 |
CLV_PCSK_PC1ET2_1 | 311 | 313 | PF00082 | 0.693 |
CLV_PCSK_SKI1_1 | 133 | 137 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 143 | 147 | PF00082 | 0.336 |
CLV_PCSK_SKI1_1 | 229 | 233 | PF00082 | 0.441 |
CLV_PCSK_SKI1_1 | 35 | 39 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 367 | 371 | PF00082 | 0.570 |
CLV_Separin_Metazoa | 68 | 72 | PF03568 | 0.472 |
DEG_APCC_DBOX_1 | 242 | 250 | PF00400 | 0.495 |
DEG_APCC_DBOX_1 | 445 | 453 | PF00400 | 0.566 |
DEG_SPOP_SBC_1 | 330 | 334 | PF00917 | 0.773 |
DOC_CYCLIN_RxL_1 | 364 | 371 | PF00134 | 0.320 |
DOC_CYCLIN_yCln2_LP_2 | 422 | 428 | PF00134 | 0.510 |
DOC_MAPK_gen_1 | 35 | 45 | PF00069 | 0.451 |
DOC_MAPK_MEF2A_6 | 156 | 165 | PF00069 | 0.455 |
DOC_MAPK_MEF2A_6 | 229 | 238 | PF00069 | 0.380 |
DOC_MAPK_RevD_3 | 358 | 373 | PF00069 | 0.579 |
DOC_PP1_RVXF_1 | 154 | 160 | PF00149 | 0.446 |
DOC_PP2B_LxvP_1 | 422 | 425 | PF13499 | 0.553 |
DOC_PP4_FxxP_1 | 144 | 147 | PF00568 | 0.392 |
DOC_PP4_FxxP_1 | 273 | 276 | PF00568 | 0.491 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.426 |
DOC_USP7_MATH_1 | 331 | 335 | PF00917 | 0.769 |
DOC_USP7_MATH_1 | 374 | 378 | PF00917 | 0.287 |
DOC_USP7_MATH_1 | 392 | 396 | PF00917 | 0.312 |
DOC_USP7_MATH_1 | 431 | 435 | PF00917 | 0.472 |
DOC_USP7_MATH_1 | 484 | 488 | PF00917 | 0.615 |
DOC_USP7_UBL2_3 | 31 | 35 | PF12436 | 0.466 |
DOC_WW_Pin1_4 | 157 | 162 | PF00397 | 0.441 |
DOC_WW_Pin1_4 | 258 | 263 | PF00397 | 0.601 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.564 |
LIG_14-3-3_CanoR_1 | 255 | 262 | PF00244 | 0.521 |
LIG_14-3-3_CanoR_1 | 32 | 38 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 470 | 476 | PF00244 | 0.451 |
LIG_Actin_WH2_2 | 242 | 257 | PF00022 | 0.401 |
LIG_AP2alpha_1 | 379 | 383 | PF02296 | 0.434 |
LIG_AP2alpha_2 | 184 | 186 | PF02296 | 0.453 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.719 |
LIG_CSL_BTD_1 | 158 | 161 | PF09270 | 0.435 |
LIG_deltaCOP1_diTrp_1 | 244 | 250 | PF00928 | 0.390 |
LIG_deltaCOP1_diTrp_1 | 458 | 464 | PF00928 | 0.324 |
LIG_FHA_1 | 102 | 108 | PF00498 | 0.428 |
LIG_FHA_1 | 130 | 136 | PF00498 | 0.449 |
LIG_FHA_1 | 230 | 236 | PF00498 | 0.399 |
LIG_FHA_1 | 419 | 425 | PF00498 | 0.476 |
LIG_FHA_1 | 430 | 436 | PF00498 | 0.546 |
LIG_FHA_1 | 85 | 91 | PF00498 | 0.506 |
LIG_FHA_2 | 115 | 121 | PF00498 | 0.512 |
LIG_FHA_2 | 259 | 265 | PF00498 | 0.632 |
LIG_FHA_2 | 279 | 285 | PF00498 | 0.377 |
LIG_FHA_2 | 298 | 304 | PF00498 | 0.625 |
LIG_FHA_2 | 335 | 341 | PF00498 | 0.768 |
LIG_FHA_2 | 407 | 413 | PF00498 | 0.485 |
LIG_FHA_2 | 477 | 483 | PF00498 | 0.603 |
LIG_LIR_Apic_2 | 189 | 195 | PF02991 | 0.394 |
LIG_LIR_Apic_2 | 271 | 276 | PF02991 | 0.615 |
LIG_LIR_Gen_1 | 23 | 34 | PF02991 | 0.318 |
LIG_LIR_Gen_1 | 293 | 304 | PF02991 | 0.621 |
LIG_LIR_Gen_1 | 377 | 386 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 170 | 176 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 23 | 29 | PF02991 | 0.309 |
LIG_LIR_Nem_3 | 293 | 299 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 303 | 309 | PF02991 | 0.558 |
LIG_LIR_Nem_3 | 377 | 382 | PF02991 | 0.380 |
LIG_Pex14_1 | 459 | 463 | PF04695 | 0.510 |
LIG_Pex14_2 | 379 | 383 | PF04695 | 0.434 |
LIG_Pex14_2 | 51 | 55 | PF04695 | 0.459 |
LIG_SH2_CRK | 192 | 196 | PF00017 | 0.532 |
LIG_SH2_CRK | 26 | 30 | PF00017 | 0.421 |
LIG_SH2_GRB2like | 150 | 153 | PF00017 | 0.419 |
LIG_SH2_NCK_1 | 26 | 30 | PF00017 | 0.294 |
LIG_SH2_SRC | 439 | 442 | PF00017 | 0.314 |
LIG_SH2_STAP1 | 306 | 310 | PF00017 | 0.551 |
LIG_SH2_STAP1 | 60 | 64 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 100 | 103 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 225 | 228 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 237 | 240 | PF00017 | 0.311 |
LIG_SH2_STAT5 | 439 | 442 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 463 | 466 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 60 | 63 | PF00017 | 0.421 |
LIG_SH3_3 | 155 | 161 | PF00018 | 0.411 |
LIG_SH3_3 | 425 | 431 | PF00018 | 0.558 |
LIG_SH3_3 | 442 | 448 | PF00018 | 0.510 |
LIG_TRAF2_1 | 337 | 340 | PF00917 | 0.561 |
MOD_CDK_SPK_2 | 157 | 162 | PF00069 | 0.441 |
MOD_CK1_1 | 332 | 338 | PF00069 | 0.750 |
MOD_CK2_1 | 114 | 120 | PF00069 | 0.480 |
MOD_CK2_1 | 258 | 264 | PF00069 | 0.629 |
MOD_CK2_1 | 288 | 294 | PF00069 | 0.595 |
MOD_CK2_1 | 297 | 303 | PF00069 | 0.543 |
MOD_CK2_1 | 334 | 340 | PF00069 | 0.565 |
MOD_CK2_1 | 374 | 380 | PF00069 | 0.374 |
MOD_CK2_1 | 406 | 412 | PF00069 | 0.428 |
MOD_CK2_1 | 476 | 482 | PF00069 | 0.528 |
MOD_CMANNOS | 247 | 250 | PF00535 | 0.378 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.502 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.662 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.700 |
MOD_GlcNHglycan | 353 | 357 | PF01048 | 0.414 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.473 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.421 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.477 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.426 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.451 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.577 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.477 |
MOD_GSK3_1 | 330 | 337 | PF00069 | 0.675 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.582 |
MOD_GSK3_1 | 429 | 436 | PF00069 | 0.588 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.421 |
MOD_NEK2_1 | 278 | 283 | PF00069 | 0.460 |
MOD_NEK2_1 | 305 | 310 | PF00069 | 0.577 |
MOD_NEK2_1 | 352 | 357 | PF00069 | 0.564 |
MOD_NEK2_1 | 418 | 423 | PF00069 | 0.488 |
MOD_NEK2_1 | 471 | 476 | PF00069 | 0.443 |
MOD_NEK2_2 | 250 | 255 | PF00069 | 0.371 |
MOD_NEK2_2 | 374 | 379 | PF00069 | 0.281 |
MOD_NEK2_2 | 433 | 438 | PF00069 | 0.494 |
MOD_PIKK_1 | 334 | 340 | PF00454 | 0.766 |
MOD_PIKK_1 | 447 | 453 | PF00454 | 0.550 |
MOD_PIKK_1 | 84 | 90 | PF00454 | 0.560 |
MOD_PKA_2 | 167 | 173 | PF00069 | 0.473 |
MOD_PKA_2 | 254 | 260 | PF00069 | 0.491 |
MOD_PKA_2 | 297 | 303 | PF00069 | 0.587 |
MOD_Plk_1 | 284 | 290 | PF00069 | 0.539 |
MOD_Plk_2-3 | 114 | 120 | PF00069 | 0.454 |
MOD_Plk_2-3 | 78 | 84 | PF00069 | 0.489 |
MOD_Plk_4 | 114 | 120 | PF00069 | 0.439 |
MOD_Plk_4 | 150 | 156 | PF00069 | 0.411 |
MOD_Plk_4 | 193 | 199 | PF00069 | 0.536 |
MOD_Plk_4 | 274 | 280 | PF00069 | 0.438 |
MOD_Plk_4 | 284 | 290 | PF00069 | 0.351 |
MOD_Plk_4 | 305 | 311 | PF00069 | 0.579 |
MOD_Plk_4 | 374 | 380 | PF00069 | 0.481 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.371 |
MOD_Plk_4 | 471 | 477 | PF00069 | 0.528 |
MOD_Plk_4 | 6 | 12 | PF00069 | 0.653 |
MOD_ProDKin_1 | 157 | 163 | PF00069 | 0.447 |
MOD_ProDKin_1 | 258 | 264 | PF00069 | 0.604 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.554 |
MOD_SUMO_rev_2 | 205 | 215 | PF00179 | 0.460 |
MOD_SUMO_rev_2 | 366 | 375 | PF00179 | 0.543 |
MOD_SUMO_rev_2 | 76 | 82 | PF00179 | 0.491 |
TRG_DiLeu_BaEn_1 | 114 | 119 | PF01217 | 0.572 |
TRG_DiLeu_BaLyEn_6 | 364 | 369 | PF01217 | 0.454 |
TRG_ENDOCYTIC_2 | 173 | 176 | PF00928 | 0.533 |
TRG_ENDOCYTIC_2 | 26 | 29 | PF00928 | 0.421 |
TRG_ER_diArg_1 | 365 | 368 | PF00400 | 0.321 |
TRG_NLS_MonoExtC_3 | 132 | 137 | PF00514 | 0.543 |
TRG_Pf-PMV_PEXEL_1 | 367 | 371 | PF00026 | 0.542 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8U9 | Leptomonas seymouri | 69% | 100% |
A0A0S4J099 | Bodo saltans | 26% | 100% |
A0A0S4JY56 | Bodo saltans | 45% | 96% |
A0A3Q8ICB7 | Leishmania donovani | 82% | 100% |
A4I6A2 | Leishmania infantum | 82% | 100% |
C9ZM74 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 83% |
C9ZWU9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 91% |
E9B1F7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
Q4Q6Q5 | Leishmania major | 81% | 100% |