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 |
Related structures:
AlphaFold database: A0A3S7X626
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0016925 | protein sumoylation | 7 | 1 |
GO:0018193 | peptidyl-amino acid modification | 5 | 1 |
GO:0018205 | peptidyl-lysine modification | 6 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0032446 | protein modification by small protein conjugation | 6 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 12 |
GO:0008270 | zinc ion binding | 6 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043169 | cation binding | 3 | 12 |
GO:0046872 | metal ion binding | 4 | 12 |
GO:0046914 | transition metal ion binding | 5 | 12 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0019787 | ubiquitin-like protein transferase activity | 3 | 1 |
GO:0019789 | SUMO transferase activity | 4 | 1 |
GO:0061659 | ubiquitin-like protein ligase activity | 4 | 1 |
GO:0061665 | SUMO ligase activity | 5 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 143 | 147 | PF00656 | 0.588 |
CLV_C14_Caspase3-7 | 158 | 162 | PF00656 | 0.660 |
CLV_C14_Caspase3-7 | 174 | 178 | PF00656 | 0.515 |
CLV_C14_Caspase3-7 | 404 | 408 | PF00656 | 0.580 |
CLV_NRD_NRD_1 | 13 | 15 | PF00675 | 0.797 |
CLV_NRD_NRD_1 | 135 | 137 | PF00675 | 0.616 |
CLV_NRD_NRD_1 | 192 | 194 | PF00675 | 0.791 |
CLV_NRD_NRD_1 | 316 | 318 | PF00675 | 0.425 |
CLV_NRD_NRD_1 | 424 | 426 | PF00675 | 0.614 |
CLV_NRD_NRD_1 | 91 | 93 | PF00675 | 0.555 |
CLV_PCSK_FUR_1 | 133 | 137 | PF00082 | 0.658 |
CLV_PCSK_FUR_1 | 422 | 426 | PF00082 | 0.681 |
CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.797 |
CLV_PCSK_KEX2_1 | 135 | 137 | PF00082 | 0.570 |
CLV_PCSK_KEX2_1 | 192 | 194 | PF00082 | 0.791 |
CLV_PCSK_KEX2_1 | 316 | 318 | PF00082 | 0.424 |
CLV_PCSK_KEX2_1 | 422 | 424 | PF00082 | 0.583 |
CLV_PCSK_KEX2_1 | 91 | 93 | PF00082 | 0.495 |
CLV_PCSK_PC7_1 | 419 | 425 | PF00082 | 0.579 |
CLV_PCSK_SKI1_1 | 353 | 357 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 91 | 95 | PF00082 | 0.542 |
DEG_COP1_1 | 407 | 417 | PF00400 | 0.493 |
DEG_SPOP_SBC_1 | 172 | 176 | PF00917 | 0.633 |
DEG_SPOP_SBC_1 | 378 | 382 | PF00917 | 0.510 |
DEG_SPOP_SBC_1 | 93 | 97 | PF00917 | 0.565 |
DOC_CKS1_1 | 18 | 23 | PF01111 | 0.741 |
DOC_CYCLIN_RxL_1 | 348 | 360 | PF00134 | 0.580 |
DOC_MAPK_gen_1 | 135 | 144 | PF00069 | 0.610 |
DOC_PP4_FxxP_1 | 418 | 421 | PF00568 | 0.496 |
DOC_SPAK_OSR1_1 | 387 | 391 | PF12202 | 0.482 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.813 |
DOC_USP7_MATH_1 | 125 | 129 | PF00917 | 0.456 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.735 |
DOC_USP7_MATH_1 | 271 | 275 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 320 | 324 | PF00917 | 0.510 |
DOC_USP7_MATH_1 | 426 | 430 | PF00917 | 0.704 |
DOC_USP7_MATH_1 | 450 | 454 | PF00917 | 0.735 |
DOC_USP7_MATH_1 | 52 | 56 | PF00917 | 0.486 |
DOC_WW_Pin1_4 | 17 | 22 | PF00397 | 0.720 |
DOC_WW_Pin1_4 | 195 | 200 | PF00397 | 0.764 |
DOC_WW_Pin1_4 | 216 | 221 | PF00397 | 0.794 |
DOC_WW_Pin1_4 | 241 | 246 | PF00397 | 0.679 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.794 |
LIG_14-3-3_CanoR_1 | 13 | 21 | PF00244 | 0.809 |
LIG_14-3-3_CanoR_1 | 91 | 100 | PF00244 | 0.458 |
LIG_BIR_III_4 | 307 | 311 | PF00653 | 0.539 |
LIG_BRCT_BRCA1_1 | 34 | 38 | PF00533 | 0.577 |
LIG_deltaCOP1_diTrp_1 | 311 | 318 | PF00928 | 0.409 |
LIG_deltaCOP1_diTrp_1 | 377 | 383 | PF00928 | 0.560 |
LIG_FHA_1 | 113 | 119 | PF00498 | 0.504 |
LIG_FHA_1 | 331 | 337 | PF00498 | 0.413 |
LIG_FHA_2 | 129 | 135 | PF00498 | 0.670 |
LIG_FHA_2 | 146 | 152 | PF00498 | 0.505 |
LIG_FHA_2 | 172 | 178 | PF00498 | 0.717 |
LIG_FHA_2 | 247 | 253 | PF00498 | 0.586 |
LIG_Integrin_RGDW_4 | 309 | 312 | PF00362 | 0.534 |
LIG_LIR_Apic_2 | 416 | 421 | PF02991 | 0.566 |
LIG_LIR_Gen_1 | 311 | 320 | PF02991 | 0.418 |
LIG_LIR_Gen_1 | 35 | 44 | PF02991 | 0.395 |
LIG_LIR_Gen_1 | 354 | 364 | PF02991 | 0.623 |
LIG_LIR_Gen_1 | 67 | 73 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 150 | 155 | PF02991 | 0.672 |
LIG_LIR_Nem_3 | 311 | 315 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 35 | 41 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 360 | 364 | PF02991 | 0.619 |
LIG_Pex14_1 | 379 | 383 | PF04695 | 0.494 |
LIG_Pex14_2 | 314 | 318 | PF04695 | 0.458 |
LIG_Pex14_2 | 388 | 392 | PF04695 | 0.500 |
LIG_SH2_CRK | 352 | 356 | PF00017 | 0.610 |
LIG_SH2_CRK | 361 | 365 | PF00017 | 0.586 |
LIG_SH2_CRK | 372 | 376 | PF00017 | 0.354 |
LIG_SH2_CRK | 44 | 48 | PF00017 | 0.522 |
LIG_SH2_GRB2like | 152 | 155 | PF00017 | 0.663 |
LIG_SH2_NCK_1 | 361 | 365 | PF00017 | 0.615 |
LIG_SH2_STAP1 | 152 | 156 | PF00017 | 0.680 |
LIG_SH2_STAP1 | 361 | 365 | PF00017 | 0.638 |
LIG_SH2_STAT5 | 155 | 158 | PF00017 | 0.692 |
LIG_SH2_STAT5 | 345 | 348 | PF00017 | 0.430 |
LIG_SH3_3 | 196 | 202 | PF00018 | 0.791 |
LIG_SH3_3 | 242 | 248 | PF00018 | 0.764 |
LIG_SH3_3 | 79 | 85 | PF00018 | 0.484 |
LIG_SUMO_SIM_par_1 | 115 | 121 | PF11976 | 0.477 |
LIG_TRAF2_1 | 249 | 252 | PF00917 | 0.565 |
MOD_CK1_1 | 128 | 134 | PF00069 | 0.473 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.742 |
MOD_CK1_1 | 176 | 182 | PF00069 | 0.637 |
MOD_CK1_1 | 246 | 252 | PF00069 | 0.629 |
MOD_CK1_1 | 322 | 328 | PF00069 | 0.427 |
MOD_CK1_1 | 408 | 414 | PF00069 | 0.585 |
MOD_CK1_1 | 429 | 435 | PF00069 | 0.663 |
MOD_CK2_1 | 128 | 134 | PF00069 | 0.584 |
MOD_CK2_1 | 246 | 252 | PF00069 | 0.703 |
MOD_CK2_1 | 351 | 357 | PF00069 | 0.526 |
MOD_CK2_1 | 360 | 366 | PF00069 | 0.567 |
MOD_DYRK1A_RPxSP_1 | 216 | 220 | PF00069 | 0.706 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.407 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.679 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.788 |
MOD_GlcNHglycan | 209 | 212 | PF01048 | 0.724 |
MOD_GlcNHglycan | 428 | 431 | PF01048 | 0.724 |
MOD_GlcNHglycan | 440 | 443 | PF01048 | 0.473 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.438 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.693 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.781 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.673 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.519 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.492 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.713 |
MOD_N-GLC_2 | 56 | 58 | PF02516 | 0.311 |
MOD_N-GLC_2 | 74 | 76 | PF02516 | 0.161 |
MOD_NEK2_1 | 281 | 286 | PF00069 | 0.565 |
MOD_NEK2_1 | 318 | 323 | PF00069 | 0.540 |
MOD_NEK2_1 | 351 | 356 | PF00069 | 0.554 |
MOD_PIKK_1 | 14 | 20 | PF00454 | 0.793 |
MOD_PIKK_1 | 145 | 151 | PF00454 | 0.508 |
MOD_PIKK_1 | 247 | 253 | PF00454 | 0.727 |
MOD_PIKK_1 | 271 | 277 | PF00454 | 0.474 |
MOD_PIKK_1 | 432 | 438 | PF00454 | 0.694 |
MOD_PIKK_1 | 450 | 456 | PF00454 | 0.749 |
MOD_PKA_1 | 91 | 97 | PF00069 | 0.486 |
MOD_PKA_2 | 12 | 18 | PF00069 | 0.810 |
MOD_PKA_2 | 91 | 97 | PF00069 | 0.486 |
MOD_Plk_1 | 36 | 42 | PF00069 | 0.362 |
MOD_Plk_2-3 | 360 | 366 | PF00069 | 0.647 |
MOD_Plk_4 | 330 | 336 | PF00069 | 0.411 |
MOD_Plk_4 | 408 | 414 | PF00069 | 0.562 |
MOD_Plk_4 | 65 | 71 | PF00069 | 0.475 |
MOD_ProDKin_1 | 17 | 23 | PF00069 | 0.719 |
MOD_ProDKin_1 | 195 | 201 | PF00069 | 0.763 |
MOD_ProDKin_1 | 216 | 222 | PF00069 | 0.793 |
MOD_ProDKin_1 | 241 | 247 | PF00069 | 0.681 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.795 |
MOD_SUMO_for_1 | 225 | 228 | PF00179 | 0.623 |
MOD_SUMO_for_1 | 291 | 294 | PF00179 | 0.586 |
TRG_DiLeu_BaEn_1 | 27 | 32 | PF01217 | 0.749 |
TRG_ENDOCYTIC_2 | 352 | 355 | PF00928 | 0.591 |
TRG_ENDOCYTIC_2 | 361 | 364 | PF00928 | 0.578 |
TRG_ENDOCYTIC_2 | 44 | 47 | PF00928 | 0.478 |
TRG_ER_diArg_1 | 192 | 195 | PF00400 | 0.794 |
TRG_ER_diArg_1 | 315 | 317 | PF00400 | 0.458 |
TRG_ER_diArg_1 | 421 | 424 | PF00400 | 0.581 |
TRG_ER_diArg_1 | 91 | 93 | PF00400 | 0.560 |
TRG_Pf-PMV_PEXEL_1 | 353 | 357 | PF00026 | 0.609 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P907 | Leptomonas seymouri | 65% | 73% |
A0A0S4IQ84 | Bodo saltans | 31% | 77% |
A0A1X0NSE9 | Trypanosomatidae | 40% | 99% |
A0A3R7NRN3 | Trypanosoma rangeli | 40% | 100% |
A4HKV3 | Leishmania braziliensis | 84% | 100% |
A4I8D2 | Leishmania infantum | 99% | 100% |
D0AAU1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
E9B391 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q4Q4W4 | Leishmania major | 94% | 100% |
V5B5L3 | Trypanosoma cruzi | 42% | 100% |