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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: A0A3S7WUF8
Term | Name | Level | Count |
---|---|---|---|
GO:0008152 | metabolic process | 1 | 2 |
GO:0032259 | methylation | 2 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 2 |
GO:0008168 | methyltransferase activity | 4 | 2 |
GO:0016740 | transferase activity | 2 | 2 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 448 | 452 | PF00656 | 0.769 |
CLV_NRD_NRD_1 | 364 | 366 | PF00675 | 0.476 |
CLV_NRD_NRD_1 | 434 | 436 | PF00675 | 0.780 |
CLV_NRD_NRD_1 | 469 | 471 | PF00675 | 0.640 |
CLV_PCSK_FUR_1 | 432 | 436 | PF00082 | 0.811 |
CLV_PCSK_KEX2_1 | 364 | 366 | PF00082 | 0.476 |
CLV_PCSK_KEX2_1 | 432 | 434 | PF00082 | 0.778 |
CLV_PCSK_KEX2_1 | 469 | 471 | PF00082 | 0.636 |
CLV_PCSK_SKI1_1 | 118 | 122 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 192 | 196 | PF00082 | 0.607 |
CLV_Separin_Metazoa | 429 | 433 | PF03568 | 0.684 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.461 |
DEG_SPOP_SBC_1 | 229 | 233 | PF00917 | 0.652 |
DEG_SPOP_SBC_1 | 71 | 75 | PF00917 | 0.470 |
DOC_ANK_TNKS_1 | 436 | 443 | PF00023 | 0.767 |
DOC_CKS1_1 | 243 | 248 | PF01111 | 0.586 |
DOC_CYCLIN_yCln2_LP_2 | 243 | 249 | PF00134 | 0.577 |
DOC_CYCLIN_yCln2_LP_2 | 79 | 85 | PF00134 | 0.408 |
DOC_PP1_RVXF_1 | 390 | 396 | PF00149 | 0.424 |
DOC_PP2B_LxvP_1 | 210 | 213 | PF13499 | 0.505 |
DOC_PP2B_LxvP_1 | 79 | 82 | PF13499 | 0.408 |
DOC_PP4_FxxP_1 | 425 | 428 | PF00568 | 0.721 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.586 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.451 |
DOC_USP7_MATH_1 | 223 | 227 | PF00917 | 0.442 |
DOC_USP7_MATH_1 | 229 | 233 | PF00917 | 0.498 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 352 | 356 | PF00917 | 0.548 |
DOC_USP7_MATH_1 | 418 | 422 | PF00917 | 0.786 |
DOC_USP7_MATH_1 | 455 | 459 | PF00917 | 0.787 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.476 |
DOC_USP7_UBL2_3 | 162 | 166 | PF12436 | 0.473 |
DOC_WW_Pin1_4 | 179 | 184 | PF00397 | 0.694 |
DOC_WW_Pin1_4 | 238 | 243 | PF00397 | 0.648 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.465 |
LIG_14-3-3_CanoR_1 | 111 | 121 | PF00244 | 0.342 |
LIG_14-3-3_CanoR_1 | 184 | 190 | PF00244 | 0.659 |
LIG_14-3-3_CanoR_1 | 201 | 207 | PF00244 | 0.426 |
LIG_14-3-3_CanoR_1 | 333 | 343 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 392 | 401 | PF00244 | 0.453 |
LIG_14-3-3_CanoR_1 | 60 | 70 | PF00244 | 0.408 |
LIG_BIR_III_2 | 472 | 476 | PF00653 | 0.589 |
LIG_BRCT_BRCA1_1 | 189 | 193 | PF00533 | 0.547 |
LIG_BRCT_BRCA1_1 | 421 | 425 | PF00533 | 0.798 |
LIG_eIF4E_1 | 268 | 274 | PF01652 | 0.479 |
LIG_FHA_1 | 189 | 195 | PF00498 | 0.575 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.633 |
LIG_FHA_1 | 323 | 329 | PF00498 | 0.558 |
LIG_FHA_1 | 372 | 378 | PF00498 | 0.453 |
LIG_FHA_2 | 267 | 273 | PF00498 | 0.373 |
LIG_FHA_2 | 274 | 280 | PF00498 | 0.383 |
LIG_FHA_2 | 394 | 400 | PF00498 | 0.529 |
LIG_FHA_2 | 446 | 452 | PF00498 | 0.763 |
LIG_Integrin_RGD_1 | 470 | 472 | PF01839 | 0.601 |
LIG_LIR_Apic_2 | 18 | 24 | PF02991 | 0.489 |
LIG_LIR_Apic_2 | 254 | 260 | PF02991 | 0.448 |
LIG_LIR_Apic_2 | 422 | 428 | PF02991 | 0.719 |
LIG_LIR_Gen_1 | 245 | 255 | PF02991 | 0.413 |
LIG_LIR_Gen_1 | 295 | 304 | PF02991 | 0.425 |
LIG_LIR_Gen_1 | 321 | 331 | PF02991 | 0.498 |
LIG_LIR_Gen_1 | 358 | 367 | PF02991 | 0.448 |
LIG_LIR_Gen_1 | 64 | 71 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 10 | 16 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 245 | 250 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 262 | 266 | PF02991 | 0.277 |
LIG_LIR_Nem_3 | 295 | 301 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 321 | 327 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 358 | 362 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 64 | 70 | PF02991 | 0.436 |
LIG_Pex14_2 | 148 | 152 | PF04695 | 0.481 |
LIG_SH2_CRK | 257 | 261 | PF00017 | 0.498 |
LIG_SH2_PTP2 | 249 | 252 | PF00017 | 0.468 |
LIG_SH2_PTP2 | 359 | 362 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 249 | 252 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 268 | 271 | PF00017 | 0.193 |
LIG_SH2_STAT5 | 359 | 362 | PF00017 | 0.448 |
LIG_SH3_2 | 428 | 433 | PF14604 | 0.720 |
LIG_SH3_3 | 424 | 430 | PF00018 | 0.813 |
LIG_SH3_3 | 6 | 12 | PF00018 | 0.422 |
LIG_SH3_3 | 79 | 85 | PF00018 | 0.478 |
LIG_SUMO_SIM_par_1 | 226 | 235 | PF11976 | 0.432 |
LIG_TRFH_1 | 67 | 71 | PF08558 | 0.388 |
LIG_TYR_ITIM | 357 | 362 | PF00017 | 0.486 |
LIG_WW_3 | 429 | 433 | PF00397 | 0.722 |
MOD_CDK_SPK_2 | 179 | 184 | PF00069 | 0.660 |
MOD_CDK_SPxK_1 | 238 | 244 | PF00069 | 0.536 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.465 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.670 |
MOD_CK1_1 | 338 | 344 | PF00069 | 0.568 |
MOD_CK1_1 | 355 | 361 | PF00069 | 0.490 |
MOD_CK1_1 | 72 | 78 | PF00069 | 0.443 |
MOD_CK2_1 | 266 | 272 | PF00069 | 0.382 |
MOD_CK2_1 | 338 | 344 | PF00069 | 0.575 |
MOD_CK2_1 | 393 | 399 | PF00069 | 0.504 |
MOD_GlcNHglycan | 213 | 216 | PF01048 | 0.541 |
MOD_GlcNHglycan | 340 | 343 | PF01048 | 0.625 |
MOD_GlcNHglycan | 41 | 44 | PF01048 | 0.444 |
MOD_GlcNHglycan | 410 | 413 | PF01048 | 0.721 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.695 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.408 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.233 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.481 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.567 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.616 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.628 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.451 |
MOD_N-GLC_1 | 185 | 190 | PF02516 | 0.611 |
MOD_N-GLC_1 | 31 | 36 | PF02516 | 0.485 |
MOD_N-GLC_2 | 285 | 287 | PF02516 | 0.389 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.537 |
MOD_NEK2_1 | 206 | 211 | PF00069 | 0.381 |
MOD_NEK2_1 | 266 | 271 | PF00069 | 0.382 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.379 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.457 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.332 |
MOD_PKA_1 | 433 | 439 | PF00069 | 0.792 |
MOD_PKA_2 | 388 | 394 | PF00069 | 0.402 |
MOD_PKA_2 | 408 | 414 | PF00069 | 0.710 |
MOD_PKA_2 | 433 | 439 | PF00069 | 0.784 |
MOD_Plk_1 | 185 | 191 | PF00069 | 0.515 |
MOD_Plk_1 | 31 | 37 | PF00069 | 0.405 |
MOD_Plk_4 | 155 | 161 | PF00069 | 0.571 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.505 |
MOD_Plk_4 | 352 | 358 | PF00069 | 0.555 |
MOD_ProDKin_1 | 179 | 185 | PF00069 | 0.694 |
MOD_ProDKin_1 | 238 | 244 | PF00069 | 0.641 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.463 |
MOD_SUMO_for_1 | 218 | 221 | PF00179 | 0.472 |
MOD_SUMO_for_1 | 401 | 404 | PF00179 | 0.635 |
MOD_SUMO_rev_2 | 303 | 311 | PF00179 | 0.490 |
TRG_ENDOCYTIC_2 | 13 | 16 | PF00928 | 0.433 |
TRG_ENDOCYTIC_2 | 249 | 252 | PF00928 | 0.428 |
TRG_ENDOCYTIC_2 | 359 | 362 | PF00928 | 0.430 |
TRG_ENDOCYTIC_2 | 368 | 371 | PF00928 | 0.463 |
TRG_ER_diArg_1 | 392 | 395 | PF00400 | 0.463 |
TRG_ER_diArg_1 | 431 | 434 | PF00400 | 0.805 |
TRG_NES_CRM1_1 | 119 | 132 | PF08389 | 0.444 |
TRG_NES_CRM1_1 | 163 | 175 | PF08389 | 0.520 |
TRG_NLS_MonoExtC_3 | 464 | 469 | PF00514 | 0.775 |
TRG_NLS_MonoExtN_4 | 465 | 470 | PF00514 | 0.814 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HWR5 | Leptomonas seymouri | 59% | 100% |
A0A1X0NSU1 | Trypanosomatidae | 40% | 100% |
A0A422N4P6 | Trypanosoma rangeli | 41% | 100% |
A4H920 | Leishmania braziliensis | 80% | 99% |
A4HXF2 | Leishmania infantum | 100% | 100% |
C9ZP24 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
E9AR47 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q4QEB6 | Leishmania major | 93% | 100% |