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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3Q8IDL2
Term | Name | Level | Count |
---|---|---|---|
GO:0006082 | organic acid metabolic process | 3 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0019752 | carboxylic acid metabolic process | 5 | 10 |
GO:0043436 | oxoacid metabolic process | 4 | 10 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0044281 | small molecule metabolic process | 2 | 10 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0016829 | lyase activity | 2 | 10 |
GO:0016830 | carbon-carbon lyase activity | 3 | 10 |
GO:0019842 | vitamin binding | 3 | 10 |
GO:0030170 | pyridoxal phosphate binding | 4 | 10 |
GO:0036094 | small molecule binding | 2 | 10 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043168 | anion binding | 3 | 10 |
GO:0070279 | vitamin B6 binding | 3 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
GO:0016831 | carboxy-lyase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 258 | 262 | PF00656 | 0.468 |
CLV_C14_Caspase3-7 | 56 | 60 | PF00656 | 0.700 |
CLV_MEL_PAP_1 | 376 | 382 | PF00089 | 0.704 |
CLV_NRD_NRD_1 | 299 | 301 | PF00675 | 0.559 |
CLV_NRD_NRD_1 | 495 | 497 | PF00675 | 0.535 |
CLV_PCSK_KEX2_1 | 140 | 142 | PF00082 | 0.635 |
CLV_PCSK_KEX2_1 | 495 | 497 | PF00082 | 0.535 |
CLV_PCSK_PC1ET2_1 | 140 | 142 | PF00082 | 0.635 |
CLV_PCSK_SKI1_1 | 106 | 110 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 285 | 289 | PF00082 | 0.719 |
CLV_PCSK_SKI1_1 | 388 | 392 | PF00082 | 0.707 |
CLV_PCSK_SKI1_1 | 40 | 44 | PF00082 | 0.650 |
CLV_PCSK_SKI1_1 | 415 | 419 | PF00082 | 0.564 |
CLV_PCSK_SKI1_1 | 540 | 544 | PF00082 | 0.706 |
DEG_APCC_DBOX_1 | 362 | 370 | PF00400 | 0.763 |
DEG_APCC_DBOX_1 | 387 | 395 | PF00400 | 0.692 |
DEG_COP1_1 | 258 | 269 | PF00400 | 0.580 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.726 |
DEG_SCF_FBW7_1 | 51 | 56 | PF00400 | 0.724 |
DOC_CKS1_1 | 320 | 325 | PF01111 | 0.630 |
DOC_MAPK_gen_1 | 495 | 503 | PF00069 | 0.523 |
DOC_MAPK_MEF2A_6 | 479 | 488 | PF00069 | 0.633 |
DOC_MAPK_MEF2A_6 | 495 | 503 | PF00069 | 0.448 |
DOC_MAPK_RevD_3 | 126 | 141 | PF00069 | 0.544 |
DOC_PP2B_LxvP_1 | 143 | 146 | PF13499 | 0.676 |
DOC_PP2B_LxvP_1 | 507 | 510 | PF13499 | 0.676 |
DOC_SPAK_OSR1_1 | 214 | 218 | PF12202 | 0.295 |
DOC_USP7_MATH_1 | 255 | 259 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 354 | 358 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 44 | 48 | PF00917 | 0.725 |
DOC_USP7_MATH_1 | 455 | 459 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 466 | 470 | PF00917 | 0.782 |
DOC_USP7_MATH_1 | 51 | 55 | PF00917 | 0.468 |
DOC_USP7_MATH_1 | 93 | 97 | PF00917 | 0.556 |
DOC_WW_Pin1_4 | 278 | 283 | PF00397 | 0.724 |
DOC_WW_Pin1_4 | 319 | 324 | PF00397 | 0.631 |
DOC_WW_Pin1_4 | 331 | 336 | PF00397 | 0.626 |
DOC_WW_Pin1_4 | 438 | 443 | PF00397 | 0.740 |
DOC_WW_Pin1_4 | 460 | 465 | PF00397 | 0.760 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.752 |
LIG_14-3-3_CanoR_1 | 132 | 138 | PF00244 | 0.444 |
LIG_14-3-3_CanoR_1 | 17 | 23 | PF00244 | 0.745 |
LIG_14-3-3_CanoR_1 | 285 | 294 | PF00244 | 0.538 |
LIG_14-3-3_CanoR_1 | 313 | 318 | PF00244 | 0.623 |
LIG_14-3-3_CanoR_1 | 379 | 387 | PF00244 | 0.677 |
LIG_14-3-3_CanoR_1 | 540 | 545 | PF00244 | 0.574 |
LIG_14-3-3_CanoR_1 | 551 | 556 | PF00244 | 0.690 |
LIG_deltaCOP1_diTrp_1 | 340 | 344 | PF00928 | 0.662 |
LIG_Dynein_DLC8_1 | 130 | 136 | PF01221 | 0.494 |
LIG_FHA_1 | 132 | 138 | PF00498 | 0.575 |
LIG_FHA_1 | 226 | 232 | PF00498 | 0.352 |
LIG_FHA_1 | 320 | 326 | PF00498 | 0.630 |
LIG_FHA_1 | 347 | 353 | PF00498 | 0.713 |
LIG_FHA_1 | 422 | 428 | PF00498 | 0.537 |
LIG_FHA_1 | 71 | 77 | PF00498 | 0.571 |
LIG_FHA_1 | 79 | 85 | PF00498 | 0.471 |
LIG_FHA_2 | 36 | 42 | PF00498 | 0.695 |
LIG_FHA_2 | 416 | 422 | PF00498 | 0.584 |
LIG_FHA_2 | 54 | 60 | PF00498 | 0.711 |
LIG_FHA_2 | 65 | 71 | PF00498 | 0.494 |
LIG_Integrin_RGD_1 | 395 | 397 | PF01839 | 0.705 |
LIG_LIR_Gen_1 | 535 | 544 | PF02991 | 0.525 |
LIG_LIR_Gen_1 | 70 | 79 | PF02991 | 0.535 |
LIG_LIR_Nem_3 | 502 | 506 | PF02991 | 0.658 |
LIG_LIR_Nem_3 | 70 | 75 | PF02991 | 0.539 |
LIG_LYPXL_S_1 | 185 | 189 | PF13949 | 0.343 |
LIG_LYPXL_yS_3 | 186 | 189 | PF13949 | 0.343 |
LIG_Pex14_2 | 211 | 215 | PF04695 | 0.295 |
LIG_RPA_C_Fungi | 424 | 436 | PF08784 | 0.629 |
LIG_SH2_CRK | 275 | 279 | PF00017 | 0.724 |
LIG_SH2_CRK | 72 | 76 | PF00017 | 0.525 |
LIG_SH2_NCK_1 | 254 | 258 | PF00017 | 0.564 |
LIG_SH2_PTP2 | 130 | 133 | PF00017 | 0.420 |
LIG_SH2_STAP1 | 166 | 170 | PF00017 | 0.407 |
LIG_SH2_STAP1 | 65 | 69 | PF00017 | 0.633 |
LIG_SH2_STAP1 | 72 | 76 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 130 | 133 | PF00017 | 0.233 |
LIG_SH2_STAT5 | 365 | 368 | PF00017 | 0.680 |
LIG_SH2_STAT5 | 544 | 547 | PF00017 | 0.650 |
LIG_SH2_STAT5 | 72 | 75 | PF00017 | 0.544 |
LIG_SH3_3 | 13 | 19 | PF00018 | 0.750 |
LIG_SH3_3 | 235 | 241 | PF00018 | 0.646 |
LIG_SH3_3 | 260 | 266 | PF00018 | 0.511 |
LIG_SH3_3 | 276 | 282 | PF00018 | 0.687 |
LIG_SH3_3 | 330 | 336 | PF00018 | 0.667 |
LIG_SH3_3 | 367 | 373 | PF00018 | 0.740 |
LIG_SUMO_SIM_anti_2 | 203 | 210 | PF11976 | 0.412 |
LIG_SUMO_SIM_par_1 | 372 | 378 | PF11976 | 0.652 |
LIG_SUMO_SIM_par_1 | 505 | 512 | PF11976 | 0.673 |
LIG_SUMO_SIM_par_1 | 72 | 78 | PF11976 | 0.462 |
LIG_TYR_ITIM | 128 | 133 | PF00017 | 0.421 |
LIG_TYR_ITIM | 273 | 278 | PF00017 | 0.672 |
LIG_WRC_WIRS_1 | 191 | 196 | PF05994 | 0.443 |
MOD_CDK_SPxxK_3 | 278 | 285 | PF00069 | 0.712 |
MOD_CK1_1 | 150 | 156 | PF00069 | 0.687 |
MOD_CK1_1 | 196 | 202 | PF00069 | 0.443 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.613 |
MOD_CK1_1 | 281 | 287 | PF00069 | 0.645 |
MOD_CK1_1 | 334 | 340 | PF00069 | 0.735 |
MOD_CK1_1 | 460 | 466 | PF00069 | 0.779 |
MOD_CK1_1 | 516 | 522 | PF00069 | 0.585 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.546 |
MOD_CK2_1 | 334 | 340 | PF00069 | 0.665 |
MOD_CK2_1 | 35 | 41 | PF00069 | 0.701 |
MOD_CK2_1 | 64 | 70 | PF00069 | 0.520 |
MOD_DYRK1A_RPxSP_1 | 49 | 53 | PF00069 | 0.726 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.799 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.445 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.412 |
MOD_GlcNHglycan | 380 | 383 | PF01048 | 0.645 |
MOD_GlcNHglycan | 451 | 454 | PF01048 | 0.747 |
MOD_GlcNHglycan | 457 | 460 | PF01048 | 0.705 |
MOD_GlcNHglycan | 469 | 472 | PF01048 | 0.569 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.581 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.609 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.202 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.757 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.384 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.413 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.457 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.569 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.665 |
MOD_GSK3_1 | 551 | 558 | PF00069 | 0.612 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.516 |
MOD_N-GLC_2 | 23 | 25 | PF02516 | 0.575 |
MOD_NEK2_1 | 194 | 199 | PF00069 | 0.202 |
MOD_NEK2_1 | 259 | 264 | PF00069 | 0.425 |
MOD_NEK2_1 | 555 | 560 | PF00069 | 0.658 |
MOD_NEK2_1 | 64 | 69 | PF00069 | 0.502 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.450 |
MOD_PIKK_1 | 131 | 137 | PF00454 | 0.501 |
MOD_PIKK_1 | 248 | 254 | PF00454 | 0.476 |
MOD_PIKK_1 | 78 | 84 | PF00454 | 0.514 |
MOD_PKA_2 | 131 | 137 | PF00069 | 0.545 |
MOD_PKA_2 | 378 | 384 | PF00069 | 0.623 |
MOD_PKA_2 | 85 | 91 | PF00069 | 0.572 |
MOD_PKB_1 | 538 | 546 | PF00069 | 0.561 |
MOD_Plk_1 | 400 | 406 | PF00069 | 0.558 |
MOD_Plk_1 | 421 | 427 | PF00069 | 0.647 |
MOD_Plk_4 | 159 | 165 | PF00069 | 0.594 |
MOD_Plk_4 | 259 | 265 | PF00069 | 0.453 |
MOD_Plk_4 | 513 | 519 | PF00069 | 0.707 |
MOD_Plk_4 | 540 | 546 | PF00069 | 0.650 |
MOD_Plk_4 | 70 | 76 | PF00069 | 0.467 |
MOD_ProDKin_1 | 278 | 284 | PF00069 | 0.723 |
MOD_ProDKin_1 | 319 | 325 | PF00069 | 0.631 |
MOD_ProDKin_1 | 331 | 337 | PF00069 | 0.624 |
MOD_ProDKin_1 | 438 | 444 | PF00069 | 0.743 |
MOD_ProDKin_1 | 460 | 466 | PF00069 | 0.759 |
MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.751 |
TRG_DiLeu_BaLyEn_6 | 201 | 206 | PF01217 | 0.478 |
TRG_DiLeu_BaLyEn_6 | 502 | 507 | PF01217 | 0.700 |
TRG_ENDOCYTIC_2 | 130 | 133 | PF00928 | 0.420 |
TRG_ENDOCYTIC_2 | 186 | 189 | PF00928 | 0.343 |
TRG_ENDOCYTIC_2 | 275 | 278 | PF00928 | 0.680 |
TRG_ENDOCYTIC_2 | 72 | 75 | PF00928 | 0.530 |
TRG_ER_diArg_1 | 495 | 497 | PF00400 | 0.560 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDL2 | Leptomonas seymouri | 45% | 77% |
A0A1X0P0L1 | Trypanosomatidae | 30% | 83% |
A0A3R7K963 | Trypanosoma rangeli | 36% | 100% |
A4H8G7 | Leishmania braziliensis | 76% | 100% |
A4HWU0 | Leishmania infantum | 99% | 100% |
C9ZW41 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 94% |
E9AQJ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4QEX8 | Leishmania major | 92% | 100% |