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: E9AQP4
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 | 280 | 284 | PF00656 | 0.475 |
CLV_C14_Caspase3-7 | 372 | 376 | PF00656 | 0.783 |
CLV_C14_Caspase3-7 | 461 | 465 | PF00656 | 0.496 |
CLV_NRD_NRD_1 | 148 | 150 | PF00675 | 0.379 |
CLV_NRD_NRD_1 | 348 | 350 | PF00675 | 0.635 |
CLV_NRD_NRD_1 | 449 | 451 | PF00675 | 0.625 |
CLV_NRD_NRD_1 | 54 | 56 | PF00675 | 0.462 |
CLV_PCSK_KEX2_1 | 148 | 150 | PF00082 | 0.379 |
CLV_PCSK_KEX2_1 | 348 | 350 | PF00082 | 0.635 |
CLV_PCSK_KEX2_1 | 54 | 56 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 78 | 82 | PF00082 | 0.480 |
DOC_ANK_TNKS_1 | 210 | 217 | PF00023 | 0.463 |
DOC_CKS1_1 | 20 | 25 | PF01111 | 0.759 |
DOC_CKS1_1 | 42 | 47 | PF01111 | 0.494 |
DOC_CYCLIN_yCln2_LP_2 | 301 | 307 | PF00134 | 0.548 |
DOC_MAPK_gen_1 | 57 | 66 | PF00069 | 0.470 |
DOC_MAPK_HePTP_8 | 289 | 301 | PF00069 | 0.611 |
DOC_MAPK_MEF2A_6 | 269 | 277 | PF00069 | 0.453 |
DOC_MAPK_MEF2A_6 | 292 | 301 | PF00069 | 0.612 |
DOC_PP4_FxxP_1 | 119 | 122 | PF00568 | 0.379 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.673 |
DOC_USP7_MATH_1 | 226 | 230 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 236 | 240 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 243 | 247 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.479 |
DOC_USP7_MATH_1 | 88 | 92 | PF00917 | 0.364 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.700 |
DOC_WW_Pin1_4 | 352 | 357 | PF00397 | 0.462 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.732 |
DOC_WW_Pin1_4 | 41 | 46 | PF00397 | 0.495 |
DOC_WW_Pin1_4 | 439 | 444 | PF00397 | 0.604 |
LIG_14-3-3_CanoR_1 | 222 | 231 | PF00244 | 0.659 |
LIG_14-3-3_CanoR_1 | 276 | 286 | PF00244 | 0.471 |
LIG_AP2alpha_2 | 187 | 189 | PF02296 | 0.448 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.744 |
LIG_BRCT_BRCA1_1 | 299 | 303 | PF00533 | 0.535 |
LIG_BRCT_BRCA1_1 | 455 | 459 | PF00533 | 0.701 |
LIG_BRCT_BRCA1_1 | 62 | 66 | PF00533 | 0.537 |
LIG_CtBP_PxDLS_1 | 296 | 300 | PF00389 | 0.495 |
LIG_deltaCOP1_diTrp_1 | 40 | 47 | PF00928 | 0.580 |
LIG_EH1_1 | 97 | 105 | PF00400 | 0.379 |
LIG_FHA_1 | 353 | 359 | PF00498 | 0.497 |
LIG_FHA_2 | 175 | 181 | PF00498 | 0.289 |
LIG_FHA_2 | 210 | 216 | PF00498 | 0.454 |
LIG_FHA_2 | 245 | 251 | PF00498 | 0.671 |
LIG_FHA_2 | 382 | 388 | PF00498 | 0.419 |
LIG_FHA_2 | 447 | 453 | PF00498 | 0.555 |
LIG_HP1_1 | 188 | 192 | PF01393 | 0.430 |
LIG_LIR_Apic_2 | 116 | 122 | PF02991 | 0.379 |
LIG_LIR_Apic_2 | 249 | 255 | PF02991 | 0.669 |
LIG_LIR_Apic_2 | 39 | 45 | PF02991 | 0.416 |
LIG_LIR_Gen_1 | 187 | 197 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 403 | 413 | PF02991 | 0.701 |
LIG_LIR_Gen_1 | 44 | 53 | PF02991 | 0.557 |
LIG_LIR_Gen_1 | 452 | 459 | PF02991 | 0.696 |
LIG_LIR_Gen_1 | 63 | 74 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 187 | 192 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 403 | 408 | PF02991 | 0.699 |
LIG_LIR_Nem_3 | 452 | 458 | PF02991 | 0.695 |
LIG_LIR_Nem_3 | 63 | 69 | PF02991 | 0.498 |
LIG_MAD2 | 423 | 431 | PF02301 | 0.412 |
LIG_MLH1_MIPbox_1 | 62 | 66 | PF16413 | 0.537 |
LIG_PCNA_PIPBox_1 | 101 | 110 | PF02747 | 0.379 |
LIG_PDZ_Class_3 | 467 | 472 | PF00595 | 0.674 |
LIG_Pex14_1 | 43 | 47 | PF04695 | 0.581 |
LIG_Pex14_2 | 455 | 459 | PF04695 | 0.701 |
LIG_Pex14_2 | 61 | 65 | PF04695 | 0.478 |
LIG_SH2_CRK | 252 | 256 | PF00017 | 0.659 |
LIG_SH2_STAP1 | 167 | 171 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 143 | 146 | PF00017 | 0.379 |
LIG_SH3_3 | 190 | 196 | PF00018 | 0.424 |
LIG_SH3_3 | 2 | 8 | PF00018 | 0.577 |
LIG_SH3_3 | 21 | 27 | PF00018 | 0.463 |
LIG_SUMO_SIM_anti_2 | 70 | 76 | PF11976 | 0.274 |
LIG_SUMO_SIM_par_1 | 295 | 300 | PF11976 | 0.499 |
LIG_SUMO_SIM_par_1 | 389 | 394 | PF11976 | 0.678 |
LIG_TRAF2_1 | 177 | 180 | PF00917 | 0.191 |
LIG_TRFH_1 | 252 | 256 | PF08558 | 0.474 |
MOD_CDK_SPxxK_3 | 4 | 11 | PF00069 | 0.682 |
MOD_CK1_1 | 246 | 252 | PF00069 | 0.593 |
MOD_CK1_1 | 351 | 357 | PF00069 | 0.566 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.681 |
MOD_CK1_1 | 439 | 445 | PF00069 | 0.773 |
MOD_CK1_1 | 454 | 460 | PF00069 | 0.551 |
MOD_CK2_1 | 106 | 112 | PF00069 | 0.348 |
MOD_CK2_1 | 123 | 129 | PF00069 | 0.281 |
MOD_CK2_1 | 174 | 180 | PF00069 | 0.191 |
MOD_CK2_1 | 209 | 215 | PF00069 | 0.433 |
MOD_CK2_1 | 381 | 387 | PF00069 | 0.423 |
MOD_CK2_1 | 446 | 452 | PF00069 | 0.570 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.630 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.379 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.657 |
MOD_GlcNHglycan | 228 | 231 | PF01048 | 0.644 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.566 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.560 |
MOD_GlcNHglycan | 279 | 282 | PF01048 | 0.569 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.679 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.530 |
MOD_GlcNHglycan | 360 | 363 | PF01048 | 0.740 |
MOD_GlcNHglycan | 371 | 374 | PF01048 | 0.684 |
MOD_GlcNHglycan | 375 | 379 | PF01048 | 0.567 |
MOD_GlcNHglycan | 460 | 463 | PF01048 | 0.514 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.357 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.379 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.379 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.723 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.495 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.686 |
MOD_GSK3_1 | 237 | 244 | PF00069 | 0.486 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.514 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.568 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.643 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.422 |
MOD_N-GLC_1 | 18 | 23 | PF02516 | 0.512 |
MOD_N-GLC_1 | 241 | 246 | PF02516 | 0.585 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.773 |
MOD_NEK2_1 | 115 | 120 | PF00069 | 0.357 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.490 |
MOD_NEK2_1 | 305 | 310 | PF00069 | 0.549 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.668 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.766 |
MOD_NEK2_1 | 458 | 463 | PF00069 | 0.704 |
MOD_NEK2_1 | 65 | 70 | PF00069 | 0.446 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.336 |
MOD_NEK2_1 | 81 | 86 | PF00069 | 0.285 |
MOD_NEK2_2 | 165 | 170 | PF00069 | 0.379 |
MOD_NEK2_2 | 203 | 208 | PF00069 | 0.468 |
MOD_PIKK_1 | 13 | 19 | PF00454 | 0.687 |
MOD_PIKK_1 | 133 | 139 | PF00454 | 0.332 |
MOD_PIKK_1 | 175 | 181 | PF00454 | 0.379 |
MOD_PIKK_1 | 88 | 94 | PF00454 | 0.379 |
MOD_PK_1 | 348 | 354 | PF00069 | 0.567 |
MOD_PKA_1 | 348 | 354 | PF00069 | 0.567 |
MOD_PKA_2 | 348 | 354 | PF00069 | 0.567 |
MOD_PKA_2 | 446 | 452 | PF00069 | 0.588 |
MOD_PKB_1 | 222 | 230 | PF00069 | 0.657 |
MOD_PKB_1 | 399 | 407 | PF00069 | 0.591 |
MOD_Plk_1 | 128 | 134 | PF00069 | 0.372 |
MOD_Plk_1 | 451 | 457 | PF00069 | 0.756 |
MOD_Plk_2-3 | 381 | 387 | PF00069 | 0.423 |
MOD_Plk_4 | 454 | 460 | PF00069 | 0.700 |
MOD_Plk_4 | 60 | 66 | PF00069 | 0.455 |
MOD_Plk_4 | 69 | 75 | PF00069 | 0.379 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.697 |
MOD_ProDKin_1 | 352 | 358 | PF00069 | 0.464 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.733 |
MOD_ProDKin_1 | 41 | 47 | PF00069 | 0.498 |
MOD_ProDKin_1 | 439 | 445 | PF00069 | 0.604 |
TRG_DiLeu_BaEn_1 | 403 | 408 | PF01217 | 0.598 |
TRG_DiLeu_BaEn_1 | 99 | 104 | PF01217 | 0.379 |
TRG_DiLeu_BaLyEn_6 | 353 | 358 | PF01217 | 0.629 |
TRG_DiLeu_BaLyEn_6 | 386 | 391 | PF01217 | 0.696 |
TRG_ENDOCYTIC_2 | 167 | 170 | PF00928 | 0.379 |
TRG_ENDOCYTIC_2 | 270 | 273 | PF00928 | 0.377 |
TRG_ER_diArg_1 | 148 | 150 | PF00400 | 0.379 |
TRG_ER_diArg_1 | 398 | 401 | PF00400 | 0.562 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PD30 | Leptomonas seymouri | 56% | 100% |
A0A3Q8IAE8 | Leishmania donovani | 90% | 96% |
A4H8K9 | Leishmania braziliensis | 77% | 100% |
A4HWY1 | Leishmania infantum | 90% | 100% |
Q4P804 | Ustilago maydis (strain 521 / FGSC 9021) | 32% | 100% |
Q4QET4 | Leishmania major | 90% | 100% |