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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
Related structures:
AlphaFold database: E9AQI3
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 4 |
GO:0006807 | nitrogen compound metabolic process | 2 | 4 |
GO:0008152 | metabolic process | 1 | 4 |
GO:0019538 | protein metabolic process | 3 | 4 |
GO:0043170 | macromolecule metabolic process | 3 | 4 |
GO:0044238 | primary metabolic process | 2 | 4 |
GO:0071704 | organic substance metabolic process | 2 | 4 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 4 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 6 |
GO:0016787 | hydrolase activity | 2 | 6 |
GO:0008233 | peptidase activity | 3 | 4 |
GO:0008236 | serine-type peptidase activity | 4 | 4 |
GO:0017171 | serine hydrolase activity | 3 | 4 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 260 | 262 | PF00675 | 0.321 |
CLV_PCSK_FUR_1 | 258 | 262 | PF00082 | 0.276 |
CLV_PCSK_KEX2_1 | 260 | 262 | PF00082 | 0.297 |
CLV_PCSK_KEX2_1 | 29 | 31 | PF00082 | 0.363 |
CLV_PCSK_KEX2_1 | 374 | 376 | PF00082 | 0.286 |
CLV_PCSK_PC1ET2_1 | 29 | 31 | PF00082 | 0.381 |
CLV_PCSK_PC1ET2_1 | 374 | 376 | PF00082 | 0.311 |
CLV_PCSK_SKI1_1 | 293 | 297 | PF00082 | 0.285 |
CLV_PCSK_SKI1_1 | 416 | 420 | PF00082 | 0.276 |
CLV_PCSK_SKI1_1 | 76 | 80 | PF00082 | 0.366 |
CLV_PCSK_SKI1_1 | 91 | 95 | PF00082 | 0.337 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.739 |
DEG_SCF_FBW7_1 | 79 | 86 | PF00400 | 0.609 |
DEG_SPOP_SBC_1 | 351 | 355 | PF00917 | 0.562 |
DOC_CKS1_1 | 80 | 85 | PF01111 | 0.672 |
DOC_CYCLIN_yCln2_LP_2 | 142 | 148 | PF00134 | 0.363 |
DOC_MAPK_DCC_7 | 412 | 420 | PF00069 | 0.476 |
DOC_MAPK_gen_1 | 244 | 253 | PF00069 | 0.544 |
DOC_MAPK_gen_1 | 374 | 380 | PF00069 | 0.537 |
DOC_MAPK_gen_1 | 73 | 81 | PF00069 | 0.530 |
DOC_MAPK_MEF2A_6 | 137 | 146 | PF00069 | 0.479 |
DOC_MAPK_MEF2A_6 | 244 | 252 | PF00069 | 0.570 |
DOC_MAPK_MEF2A_6 | 412 | 421 | PF00069 | 0.477 |
DOC_MAPK_MEF2A_6 | 63 | 70 | PF00069 | 0.525 |
DOC_MAPK_MEF2A_6 | 87 | 94 | PF00069 | 0.594 |
DOC_MAPK_NFAT4_5 | 137 | 145 | PF00069 | 0.415 |
DOC_MAPK_NFAT4_5 | 87 | 95 | PF00069 | 0.615 |
DOC_MAPK_RevD_3 | 21 | 36 | PF00069 | 0.571 |
DOC_PP1_RVXF_1 | 89 | 95 | PF00149 | 0.626 |
DOC_PP2B_LxvP_1 | 142 | 145 | PF13499 | 0.363 |
DOC_SPAK_OSR1_1 | 302 | 306 | PF12202 | 0.476 |
DOC_USP7_MATH_1 | 191 | 195 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 484 | 488 | PF00917 | 0.728 |
DOC_USP7_MATH_1 | 83 | 87 | PF00917 | 0.683 |
DOC_USP7_UBL2_3 | 25 | 29 | PF12436 | 0.562 |
DOC_WW_Pin1_4 | 128 | 133 | PF00397 | 0.710 |
DOC_WW_Pin1_4 | 411 | 416 | PF00397 | 0.517 |
DOC_WW_Pin1_4 | 478 | 483 | PF00397 | 0.702 |
DOC_WW_Pin1_4 | 485 | 490 | PF00397 | 0.771 |
DOC_WW_Pin1_4 | 79 | 84 | PF00397 | 0.562 |
LIG_14-3-3_CanoR_1 | 12 | 21 | PF00244 | 0.530 |
LIG_14-3-3_CanoR_1 | 2 | 11 | PF00244 | 0.624 |
LIG_14-3-3_CanoR_1 | 260 | 264 | PF00244 | 0.562 |
LIG_14-3-3_CanoR_1 | 293 | 298 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 375 | 379 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 385 | 391 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 42 | 46 | PF00244 | 0.543 |
LIG_14-3-3_CanoR_1 | 432 | 438 | PF00244 | 0.501 |
LIG_BIR_III_4 | 38 | 42 | PF00653 | 0.515 |
LIG_BRCT_BRCA1_1 | 367 | 371 | PF00533 | 0.513 |
LIG_deltaCOP1_diTrp_1 | 203 | 208 | PF00928 | 0.679 |
LIG_FHA_1 | 387 | 393 | PF00498 | 0.541 |
LIG_FHA_2 | 355 | 361 | PF00498 | 0.517 |
LIG_FHA_2 | 438 | 444 | PF00498 | 0.561 |
LIG_FHA_2 | 459 | 465 | PF00498 | 0.562 |
LIG_Integrin_RGD_1 | 63 | 65 | PF01839 | 0.362 |
LIG_LIR_Gen_1 | 219 | 225 | PF02991 | 0.569 |
LIG_LIR_Gen_1 | 301 | 311 | PF02991 | 0.476 |
LIG_LIR_Gen_1 | 44 | 55 | PF02991 | 0.574 |
LIG_LIR_Nem_3 | 165 | 171 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 219 | 223 | PF02991 | 0.579 |
LIG_LIR_Nem_3 | 301 | 306 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 379 | 384 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 475 | 480 | PF02991 | 0.454 |
LIG_MLH1_MIPbox_1 | 367 | 371 | PF16413 | 0.513 |
LIG_PCNA_yPIPBox_3 | 53 | 63 | PF02747 | 0.537 |
LIG_Pex14_2 | 157 | 161 | PF04695 | 0.358 |
LIG_Pex14_2 | 390 | 394 | PF04695 | 0.526 |
LIG_PTB_Apo_2 | 269 | 276 | PF02174 | 0.562 |
LIG_PTB_Phospho_1 | 269 | 275 | PF10480 | 0.562 |
LIG_SH2_CRK | 152 | 156 | PF00017 | 0.468 |
LIG_SH2_CRK | 275 | 279 | PF00017 | 0.476 |
LIG_SH2_CRK | 318 | 322 | PF00017 | 0.537 |
LIG_SH2_CRK | 477 | 481 | PF00017 | 0.475 |
LIG_SH2_NCK_1 | 220 | 224 | PF00017 | 0.542 |
LIG_SH2_PTP2 | 170 | 173 | PF00017 | 0.262 |
LIG_SH2_PTP2 | 237 | 240 | PF00017 | 0.550 |
LIG_SH2_SRC | 220 | 223 | PF00017 | 0.539 |
LIG_SH2_SRC | 237 | 240 | PF00017 | 0.521 |
LIG_SH2_STAP1 | 376 | 380 | PF00017 | 0.487 |
LIG_SH2_STAP1 | 466 | 470 | PF00017 | 0.534 |
LIG_SH2_STAT3 | 316 | 319 | PF00017 | 0.373 |
LIG_SH2_STAT3 | 370 | 373 | PF00017 | 0.562 |
LIG_SH2_STAT5 | 170 | 173 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 175 | 178 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 231 | 234 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 237 | 240 | PF00017 | 0.520 |
LIG_SH2_STAT5 | 370 | 373 | PF00017 | 0.483 |
LIG_SH2_STAT5 | 448 | 451 | PF00017 | 0.501 |
LIG_SH2_STAT5 | 59 | 62 | PF00017 | 0.523 |
LIG_SH3_2 | 239 | 244 | PF14604 | 0.644 |
LIG_SH3_3 | 235 | 241 | PF00018 | 0.507 |
LIG_SH3_3 | 483 | 489 | PF00018 | 0.760 |
LIG_SUMO_SIM_par_1 | 362 | 368 | PF11976 | 0.562 |
LIG_TYR_ITIM | 150 | 155 | PF00017 | 0.439 |
LIG_TYR_ITIM | 218 | 223 | PF00017 | 0.537 |
LIG_UBA3_1 | 23 | 29 | PF00899 | 0.553 |
LIG_WW_1 | 184 | 187 | PF00397 | 0.550 |
MOD_CDK_SPK_2 | 411 | 416 | PF00069 | 0.517 |
MOD_CDK_SPxxK_3 | 485 | 492 | PF00069 | 0.584 |
MOD_CK1_1 | 131 | 137 | PF00069 | 0.683 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.710 |
MOD_CK1_1 | 194 | 200 | PF00069 | 0.688 |
MOD_CK1_1 | 485 | 491 | PF00069 | 0.685 |
MOD_CK2_1 | 3 | 9 | PF00069 | 0.751 |
MOD_CK2_1 | 437 | 443 | PF00069 | 0.547 |
MOD_CK2_1 | 484 | 490 | PF00069 | 0.733 |
MOD_CMANNOS | 205 | 208 | PF00535 | 0.481 |
MOD_CMANNOS | 391 | 394 | PF00535 | 0.362 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.553 |
MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.474 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.352 |
MOD_GlcNHglycan | 354 | 357 | PF01048 | 0.355 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.362 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.734 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.676 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.471 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.476 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.581 |
MOD_GSK3_1 | 478 | 485 | PF00069 | 0.724 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.513 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.629 |
MOD_N-GLC_1 | 12 | 17 | PF02516 | 0.432 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.662 |
MOD_NEK2_1 | 311 | 316 | PF00069 | 0.496 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.460 |
MOD_NEK2_1 | 365 | 370 | PF00069 | 0.545 |
MOD_NEK2_1 | 424 | 429 | PF00069 | 0.581 |
MOD_NEK2_1 | 437 | 442 | PF00069 | 0.427 |
MOD_NEK2_1 | 458 | 463 | PF00069 | 0.554 |
MOD_NEK2_1 | 92 | 97 | PF00069 | 0.569 |
MOD_NEK2_2 | 41 | 46 | PF00069 | 0.553 |
MOD_PK_1 | 374 | 380 | PF00069 | 0.511 |
MOD_PKA_1 | 374 | 380 | PF00069 | 0.554 |
MOD_PKA_2 | 124 | 130 | PF00069 | 0.739 |
MOD_PKA_2 | 259 | 265 | PF00069 | 0.554 |
MOD_PKA_2 | 374 | 380 | PF00069 | 0.512 |
MOD_PKA_2 | 41 | 47 | PF00069 | 0.532 |
MOD_PKA_2 | 431 | 437 | PF00069 | 0.501 |
MOD_PKB_1 | 10 | 18 | PF00069 | 0.707 |
MOD_Plk_1 | 12 | 18 | PF00069 | 0.708 |
MOD_Plk_1 | 466 | 472 | PF00069 | 0.573 |
MOD_Plk_2-3 | 259 | 265 | PF00069 | 0.562 |
MOD_Plk_4 | 131 | 137 | PF00069 | 0.582 |
MOD_Plk_4 | 19 | 25 | PF00069 | 0.559 |
MOD_Plk_4 | 329 | 335 | PF00069 | 0.501 |
MOD_Plk_4 | 354 | 360 | PF00069 | 0.581 |
MOD_Plk_4 | 386 | 392 | PF00069 | 0.495 |
MOD_Plk_4 | 424 | 430 | PF00069 | 0.560 |
MOD_Plk_4 | 466 | 472 | PF00069 | 0.599 |
MOD_Plk_4 | 55 | 61 | PF00069 | 0.497 |
MOD_ProDKin_1 | 128 | 134 | PF00069 | 0.705 |
MOD_ProDKin_1 | 411 | 417 | PF00069 | 0.517 |
MOD_ProDKin_1 | 478 | 484 | PF00069 | 0.710 |
MOD_ProDKin_1 | 485 | 491 | PF00069 | 0.772 |
MOD_ProDKin_1 | 79 | 85 | PF00069 | 0.562 |
MOD_SUMO_rev_2 | 439 | 447 | PF00179 | 0.487 |
MOD_SUMO_rev_2 | 69 | 78 | PF00179 | 0.581 |
TRG_DiLeu_BaLyEn_6 | 142 | 147 | PF01217 | 0.391 |
TRG_DiLeu_BaLyEn_6 | 88 | 93 | PF01217 | 0.620 |
TRG_ENDOCYTIC_2 | 152 | 155 | PF00928 | 0.399 |
TRG_ENDOCYTIC_2 | 170 | 173 | PF00928 | 0.227 |
TRG_ENDOCYTIC_2 | 220 | 223 | PF00928 | 0.536 |
TRG_ENDOCYTIC_2 | 275 | 278 | PF00928 | 0.476 |
TRG_ENDOCYTIC_2 | 318 | 321 | PF00928 | 0.487 |
TRG_ENDOCYTIC_2 | 47 | 50 | PF00928 | 0.562 |
TRG_ENDOCYTIC_2 | 477 | 480 | PF00928 | 0.651 |
TRG_ER_diLys_1 | 492 | 495 | PF00400 | 0.773 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0G5 | Leptomonas seymouri | 76% | 98% |
A0A0S4IJD1 | Bodo saltans | 47% | 98% |
A0A1X0NHG0 | Trypanosomatidae | 57% | 100% |
A0A3S5H6W8 | Leishmania donovani | 94% | 100% |
A0A422N2H5 | Trypanosoma rangeli | 58% | 100% |
A4H8F2 | Leishmania braziliensis | 87% | 100% |
A4HWS5 | Leishmania infantum | 94% | 100% |
C9ZW49 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 56% | 100% |
Q4QEZ4 | Leishmania major | 93% | 100% |
V5B955 | Trypanosoma cruzi | 58% | 100% |