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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0008180 | COP9 signalosome | 3 | 7 |
GO:0032991 | protein-containing complex | 1 | 7 |
GO:0140513 | nuclear protein-containing complex | 2 | 7 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3Q8IAE8
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0019538 | protein metabolic process | 3 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 7 |
GO:0000338 | protein deneddylation | 6 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0070646 | protein modification by small protein removal | 5 | 1 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0004175 | endopeptidase activity | 4 | 7 |
GO:0004222 | metalloendopeptidase activity | 5 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0008233 | peptidase activity | 3 | 7 |
GO:0008237 | metallopeptidase activity | 4 | 7 |
GO:0016787 | hydrolase activity | 2 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043169 | cation binding | 3 | 7 |
GO:0046872 | metal ion binding | 4 | 7 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 7 |
GO:0019783 | ubiquitin-like protein peptidase activity | 4 | 1 |
GO:0019784 | deNEDDylase activity | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 179 | 183 | PF00656 | 0.222 |
CLV_C14_Caspase3-7 | 230 | 234 | PF00656 | 0.601 |
CLV_C14_Caspase3-7 | 281 | 285 | PF00656 | 0.419 |
CLV_C14_Caspase3-7 | 373 | 377 | PF00656 | 0.678 |
CLV_NRD_NRD_1 | 149 | 151 | PF00675 | 0.288 |
CLV_NRD_NRD_1 | 349 | 351 | PF00675 | 0.740 |
CLV_NRD_NRD_1 | 463 | 465 | PF00675 | 0.539 |
CLV_NRD_NRD_1 | 474 | 476 | PF00675 | 0.485 |
CLV_NRD_NRD_1 | 489 | 491 | PF00675 | 0.408 |
CLV_NRD_NRD_1 | 55 | 57 | PF00675 | 0.373 |
CLV_PCSK_KEX2_1 | 149 | 151 | PF00082 | 0.288 |
CLV_PCSK_KEX2_1 | 349 | 351 | PF00082 | 0.740 |
CLV_PCSK_KEX2_1 | 437 | 439 | PF00082 | 0.666 |
CLV_PCSK_KEX2_1 | 463 | 465 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 489 | 491 | PF00082 | 0.422 |
CLV_PCSK_KEX2_1 | 55 | 57 | PF00082 | 0.373 |
CLV_PCSK_PC1ET2_1 | 437 | 439 | PF00082 | 0.646 |
CLV_PCSK_SKI1_1 | 79 | 83 | PF00082 | 0.376 |
CLV_Separin_Metazoa | 397 | 401 | PF03568 | 0.460 |
DEG_SCF_FBW7_1 | 20 | 26 | PF00400 | 0.590 |
DOC_ANK_TNKS_1 | 211 | 218 | PF00023 | 0.374 |
DOC_CKS1_1 | 20 | 25 | PF01111 | 0.677 |
DOC_CKS1_1 | 43 | 48 | PF01111 | 0.422 |
DOC_CYCLIN_yCln2_LP_2 | 302 | 308 | PF00134 | 0.454 |
DOC_MAPK_gen_1 | 31 | 38 | PF00069 | 0.423 |
DOC_MAPK_gen_1 | 58 | 67 | PF00069 | 0.395 |
DOC_MAPK_HePTP_8 | 290 | 302 | PF00069 | 0.507 |
DOC_MAPK_MEF2A_6 | 270 | 278 | PF00069 | 0.379 |
DOC_MAPK_MEF2A_6 | 293 | 302 | PF00069 | 0.508 |
DOC_PP4_FxxP_1 | 120 | 123 | PF00568 | 0.288 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.634 |
DOC_USP7_MATH_1 | 227 | 231 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.697 |
DOC_USP7_MATH_1 | 244 | 248 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 331 | 335 | PF00917 | 0.514 |
DOC_USP7_MATH_1 | 343 | 347 | PF00917 | 0.439 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.354 |
DOC_USP7_MATH_1 | 89 | 93 | PF00917 | 0.288 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 237 | 242 | PF00397 | 0.551 |
DOC_WW_Pin1_4 | 337 | 342 | PF00397 | 0.617 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 42 | 47 | PF00397 | 0.487 |
LIG_14-3-3_CanoR_1 | 223 | 232 | PF00244 | 0.638 |
LIG_14-3-3_CanoR_1 | 277 | 287 | PF00244 | 0.384 |
LIG_14-3-3_CanoR_1 | 33 | 37 | PF00244 | 0.405 |
LIG_Actin_WH2_2 | 187 | 204 | PF00022 | 0.322 |
LIG_AP2alpha_2 | 188 | 190 | PF02296 | 0.357 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.680 |
LIG_BRCT_BRCA1_1 | 300 | 304 | PF00533 | 0.433 |
LIG_BRCT_BRCA1_1 | 456 | 460 | PF00533 | 0.646 |
LIG_BRCT_BRCA1_1 | 63 | 67 | PF00533 | 0.442 |
LIG_CtBP_PxDLS_1 | 297 | 301 | PF00389 | 0.420 |
LIG_deltaCOP1_diTrp_1 | 41 | 48 | PF00928 | 0.483 |
LIG_EH1_1 | 98 | 106 | PF00400 | 0.288 |
LIG_FHA_1 | 393 | 399 | PF00498 | 0.520 |
LIG_FHA_2 | 177 | 183 | PF00498 | 0.248 |
LIG_FHA_2 | 211 | 217 | PF00498 | 0.363 |
LIG_FHA_2 | 246 | 252 | PF00498 | 0.611 |
LIG_HP1_1 | 189 | 193 | PF01393 | 0.339 |
LIG_LIR_Apic_2 | 117 | 123 | PF02991 | 0.288 |
LIG_LIR_Apic_2 | 250 | 256 | PF02991 | 0.593 |
LIG_LIR_Apic_2 | 40 | 46 | PF02991 | 0.394 |
LIG_LIR_Gen_1 | 188 | 198 | PF02991 | 0.342 |
LIG_LIR_Gen_1 | 404 | 414 | PF02991 | 0.600 |
LIG_LIR_Gen_1 | 45 | 54 | PF02991 | 0.504 |
LIG_LIR_Gen_1 | 453 | 460 | PF02991 | 0.615 |
LIG_LIR_Gen_1 | 64 | 75 | PF02991 | 0.179 |
LIG_LIR_Nem_3 | 188 | 193 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 404 | 409 | PF02991 | 0.596 |
LIG_LIR_Nem_3 | 453 | 459 | PF02991 | 0.613 |
LIG_LIR_Nem_3 | 64 | 70 | PF02991 | 0.433 |
LIG_MLH1_MIPbox_1 | 63 | 67 | PF16413 | 0.436 |
LIG_PCNA_PIPBox_1 | 102 | 111 | PF02747 | 0.288 |
LIG_Pex14_1 | 44 | 48 | PF04695 | 0.482 |
LIG_Pex14_2 | 456 | 460 | PF04695 | 0.622 |
LIG_Pex14_2 | 62 | 66 | PF04695 | 0.403 |
LIG_SH2_CRK | 253 | 257 | PF00017 | 0.653 |
LIG_SH2_STAP1 | 168 | 172 | PF00017 | 0.288 |
LIG_SH2_STAT5 | 144 | 147 | PF00017 | 0.288 |
LIG_SH3_3 | 191 | 197 | PF00018 | 0.333 |
LIG_SH3_3 | 302 | 308 | PF00018 | 0.514 |
LIG_SUMO_SIM_par_1 | 296 | 301 | PF11976 | 0.419 |
LIG_SUMO_SIM_par_1 | 390 | 395 | PF11976 | 0.556 |
LIG_TRAF2_1 | 467 | 470 | PF00917 | 0.665 |
LIG_TRFH_1 | 253 | 257 | PF08558 | 0.444 |
MOD_CDK_SPxxK_3 | 4 | 11 | PF00069 | 0.636 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.556 |
MOD_CK1_1 | 240 | 246 | PF00069 | 0.641 |
MOD_CK1_1 | 247 | 253 | PF00069 | 0.525 |
MOD_CK1_1 | 352 | 358 | PF00069 | 0.508 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.636 |
MOD_CK1_1 | 443 | 449 | PF00069 | 0.654 |
MOD_CK1_1 | 455 | 461 | PF00069 | 0.675 |
MOD_CK2_1 | 107 | 113 | PF00069 | 0.446 |
MOD_CK2_1 | 124 | 130 | PF00069 | 0.213 |
MOD_CK2_1 | 210 | 216 | PF00069 | 0.341 |
MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.288 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.712 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.646 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.659 |
MOD_GlcNHglycan | 280 | 283 | PF01048 | 0.471 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.605 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.550 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.459 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.620 |
MOD_GlcNHglycan | 372 | 375 | PF01048 | 0.565 |
MOD_GlcNHglycan | 376 | 380 | PF01048 | 0.494 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.298 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.293 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.312 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.704 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.428 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.695 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.650 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.427 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.572 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.498 |
MOD_GSK3_1 | 439 | 446 | PF00069 | 0.625 |
MOD_GSK3_1 | 454 | 461 | PF00069 | 0.667 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.322 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.631 |
MOD_N-GLC_2 | 314 | 316 | PF02516 | 0.426 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.638 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.288 |
MOD_NEK2_1 | 298 | 303 | PF00069 | 0.435 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.574 |
MOD_NEK2_1 | 359 | 364 | PF00069 | 0.727 |
MOD_NEK2_1 | 459 | 464 | PF00069 | 0.631 |
MOD_NEK2_1 | 66 | 71 | PF00069 | 0.379 |
MOD_NEK2_1 | 74 | 79 | PF00069 | 0.261 |
MOD_NEK2_1 | 82 | 87 | PF00069 | 0.222 |
MOD_NEK2_2 | 166 | 171 | PF00069 | 0.288 |
MOD_NEK2_2 | 197 | 202 | PF00069 | 0.350 |
MOD_NEK2_2 | 204 | 209 | PF00069 | 0.428 |
MOD_PIKK_1 | 13 | 19 | PF00454 | 0.631 |
MOD_PIKK_1 | 134 | 140 | PF00454 | 0.288 |
MOD_PIKK_1 | 176 | 182 | PF00454 | 0.288 |
MOD_PIKK_1 | 89 | 95 | PF00454 | 0.288 |
MOD_PK_1 | 349 | 355 | PF00069 | 0.515 |
MOD_PKA_1 | 349 | 355 | PF00069 | 0.515 |
MOD_PKA_2 | 180 | 186 | PF00069 | 0.227 |
MOD_PKA_2 | 32 | 38 | PF00069 | 0.409 |
MOD_PKA_2 | 349 | 355 | PF00069 | 0.567 |
MOD_PKB_1 | 223 | 231 | PF00069 | 0.624 |
MOD_PKB_1 | 400 | 408 | PF00069 | 0.515 |
MOD_Plk_1 | 129 | 135 | PF00069 | 0.284 |
MOD_Plk_1 | 452 | 458 | PF00069 | 0.653 |
MOD_Plk_4 | 455 | 461 | PF00069 | 0.619 |
MOD_Plk_4 | 61 | 67 | PF00069 | 0.479 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.543 |
MOD_ProDKin_1 | 237 | 243 | PF00069 | 0.552 |
MOD_ProDKin_1 | 337 | 343 | PF00069 | 0.617 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.678 |
MOD_ProDKin_1 | 42 | 48 | PF00069 | 0.489 |
TRG_AP2beta_CARGO_1 | 453 | 463 | PF09066 | 0.578 |
TRG_DiLeu_BaEn_1 | 100 | 105 | PF01217 | 0.288 |
TRG_DiLeu_BaEn_1 | 404 | 409 | PF01217 | 0.508 |
TRG_DiLeu_BaLyEn_6 | 354 | 359 | PF01217 | 0.525 |
TRG_DiLeu_BaLyEn_6 | 387 | 392 | PF01217 | 0.568 |
TRG_ENDOCYTIC_2 | 168 | 171 | PF00928 | 0.288 |
TRG_ENDOCYTIC_2 | 271 | 274 | PF00928 | 0.376 |
TRG_ER_diArg_1 | 149 | 151 | PF00400 | 0.288 |
TRG_ER_diArg_1 | 399 | 402 | PF00400 | 0.480 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PD30 | Leptomonas seymouri | 59% | 100% |
A4H8K9 | Leishmania braziliensis | 79% | 100% |
A4HWY1 | Leishmania infantum | 100% | 100% |
E9AQP4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4P804 | Ustilago maydis (strain 521 / FGSC 9021) | 31% | 100% |
Q4QET4 | Leishmania major | 94% | 100% |