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:0005840 | ribosome | 5 | 3 |
GO:0043226 | organelle | 2 | 3 |
GO:0043228 | non-membrane-bounded organelle | 3 | 3 |
GO:0043229 | intracellular organelle | 3 | 3 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
Related structures:
AlphaFold database: Q4QGD9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 321 | 325 | PF00656 | 0.469 |
CLV_NRD_NRD_1 | 136 | 138 | PF00675 | 0.609 |
CLV_NRD_NRD_1 | 146 | 148 | PF00675 | 0.551 |
CLV_NRD_NRD_1 | 154 | 156 | PF00675 | 0.595 |
CLV_NRD_NRD_1 | 167 | 169 | PF00675 | 0.603 |
CLV_NRD_NRD_1 | 452 | 454 | PF00675 | 0.514 |
CLV_PCSK_FUR_1 | 144 | 148 | PF00082 | 0.613 |
CLV_PCSK_KEX2_1 | 146 | 148 | PF00082 | 0.605 |
CLV_PCSK_KEX2_1 | 154 | 156 | PF00082 | 0.692 |
CLV_PCSK_KEX2_1 | 167 | 169 | PF00082 | 0.649 |
CLV_PCSK_KEX2_1 | 435 | 437 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 452 | 454 | PF00082 | 0.578 |
CLV_PCSK_PC1ET2_1 | 435 | 437 | PF00082 | 0.493 |
CLV_PCSK_SKI1_1 | 12 | 16 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 154 | 158 | PF00082 | 0.658 |
CLV_PCSK_SKI1_1 | 429 | 433 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 79 | 83 | PF00082 | 0.667 |
DEG_SCF_TRCP1_1 | 209 | 215 | PF00400 | 0.585 |
DEG_SPOP_SBC_1 | 103 | 107 | PF00917 | 0.785 |
DOC_CKS1_1 | 81 | 86 | PF01111 | 0.761 |
DOC_CKS1_1 | 97 | 102 | PF01111 | 0.524 |
DOC_MAPK_gen_1 | 135 | 143 | PF00069 | 0.583 |
DOC_MAPK_MEF2A_6 | 135 | 143 | PF00069 | 0.637 |
DOC_PP4_FxxP_1 | 303 | 306 | PF00568 | 0.491 |
DOC_USP7_MATH_1 | 101 | 105 | PF00917 | 0.783 |
DOC_USP7_MATH_1 | 366 | 370 | PF00917 | 0.593 |
DOC_WW_Pin1_4 | 241 | 246 | PF00397 | 0.440 |
DOC_WW_Pin1_4 | 289 | 294 | PF00397 | 0.473 |
DOC_WW_Pin1_4 | 377 | 382 | PF00397 | 0.486 |
DOC_WW_Pin1_4 | 80 | 85 | PF00397 | 0.740 |
DOC_WW_Pin1_4 | 96 | 101 | PF00397 | 0.623 |
LIG_14-3-3_CanoR_1 | 162 | 169 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 339 | 343 | PF00244 | 0.610 |
LIG_14-3-3_CanoR_1 | 436 | 440 | PF00244 | 0.432 |
LIG_14-3-3_CanoR_1 | 67 | 73 | PF00244 | 0.729 |
LIG_APCC_ABBA_1 | 275 | 280 | PF00400 | 0.384 |
LIG_BRCT_BRCA1_1 | 106 | 110 | PF00533 | 0.764 |
LIG_deltaCOP1_diTrp_1 | 232 | 239 | PF00928 | 0.556 |
LIG_EH1_1 | 355 | 363 | PF00400 | 0.635 |
LIG_eIF4E_1 | 451 | 457 | PF01652 | 0.567 |
LIG_FHA_1 | 405 | 411 | PF00498 | 0.643 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.766 |
LIG_FHA_2 | 172 | 178 | PF00498 | 0.619 |
LIG_FHA_2 | 194 | 200 | PF00498 | 0.570 |
LIG_FHA_2 | 241 | 247 | PF00498 | 0.467 |
LIG_FHA_2 | 319 | 325 | PF00498 | 0.614 |
LIG_Integrin_RGD_1 | 54 | 56 | PF01839 | 0.607 |
LIG_LIR_Apic_2 | 301 | 306 | PF02991 | 0.521 |
LIG_LIR_Gen_1 | 196 | 204 | PF02991 | 0.580 |
LIG_LIR_Gen_1 | 236 | 245 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 13 | 18 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 150 | 156 | PF02991 | 0.616 |
LIG_LIR_Nem_3 | 196 | 200 | PF02991 | 0.558 |
LIG_LIR_Nem_3 | 236 | 240 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 460 | 466 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 56 | 62 | PF02991 | 0.601 |
LIG_MYND_1 | 377 | 381 | PF01753 | 0.528 |
LIG_Pex14_2 | 11 | 15 | PF04695 | 0.539 |
LIG_Pex14_2 | 229 | 233 | PF04695 | 0.595 |
LIG_SH2_CRK | 153 | 157 | PF00017 | 0.610 |
LIG_SH2_CRK | 26 | 30 | PF00017 | 0.480 |
LIG_SH2_STAP1 | 278 | 282 | PF00017 | 0.501 |
LIG_SH2_STAP1 | 421 | 425 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 172 | 175 | PF00017 | 0.612 |
LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.665 |
LIG_SH2_STAT5 | 268 | 271 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 390 | 393 | PF00017 | 0.391 |
LIG_SH3_2 | 114 | 119 | PF14604 | 0.633 |
LIG_SH3_3 | 11 | 17 | PF00018 | 0.545 |
LIG_SH3_3 | 111 | 117 | PF00018 | 0.428 |
LIG_SH3_3 | 375 | 381 | PF00018 | 0.416 |
LIG_SH3_3 | 91 | 97 | PF00018 | 0.796 |
LIG_TRAF2_1 | 174 | 177 | PF00917 | 0.592 |
MOD_CDK_SPxxK_3 | 241 | 248 | PF00069 | 0.486 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.787 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.588 |
MOD_CK1_1 | 207 | 213 | PF00069 | 0.558 |
MOD_CK1_1 | 289 | 295 | PF00069 | 0.525 |
MOD_CK1_1 | 320 | 326 | PF00069 | 0.580 |
MOD_CK1_1 | 438 | 444 | PF00069 | 0.435 |
MOD_CK2_1 | 171 | 177 | PF00069 | 0.622 |
MOD_CK2_1 | 240 | 246 | PF00069 | 0.506 |
MOD_CK2_1 | 278 | 284 | PF00069 | 0.460 |
MOD_Cter_Amidation | 144 | 147 | PF01082 | 0.462 |
MOD_Cter_Amidation | 433 | 436 | PF01082 | 0.504 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.603 |
MOD_GlcNHglycan | 209 | 212 | PF01048 | 0.531 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.580 |
MOD_GlcNHglycan | 280 | 283 | PF01048 | 0.499 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.547 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.597 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.529 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.578 |
MOD_GSK3_1 | 417 | 424 | PF00069 | 0.444 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.456 |
MOD_N-GLC_1 | 181 | 186 | PF02516 | 0.715 |
MOD_N-GLC_1 | 289 | 294 | PF02516 | 0.473 |
MOD_N-GLC_1 | 318 | 323 | PF02516 | 0.533 |
MOD_N-GLC_1 | 404 | 409 | PF02516 | 0.661 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.783 |
MOD_NEK2_1 | 200 | 205 | PF00069 | 0.691 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.511 |
MOD_NEK2_1 | 240 | 245 | PF00069 | 0.514 |
MOD_NEK2_1 | 392 | 397 | PF00069 | 0.482 |
MOD_NEK2_1 | 46 | 51 | PF00069 | 0.471 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.708 |
MOD_PIKK_1 | 392 | 398 | PF00454 | 0.523 |
MOD_PKA_1 | 154 | 160 | PF00069 | 0.695 |
MOD_PKA_1 | 435 | 441 | PF00069 | 0.504 |
MOD_PKA_2 | 154 | 160 | PF00069 | 0.615 |
MOD_PKA_2 | 161 | 167 | PF00069 | 0.654 |
MOD_PKA_2 | 207 | 213 | PF00069 | 0.558 |
MOD_PKA_2 | 338 | 344 | PF00069 | 0.583 |
MOD_PKA_2 | 435 | 441 | PF00069 | 0.444 |
MOD_Plk_1 | 283 | 289 | PF00069 | 0.589 |
MOD_Plk_1 | 366 | 372 | PF00069 | 0.588 |
MOD_Plk_4 | 225 | 231 | PF00069 | 0.627 |
MOD_Plk_4 | 324 | 330 | PF00069 | 0.546 |
MOD_Plk_4 | 357 | 363 | PF00069 | 0.571 |
MOD_Plk_4 | 421 | 427 | PF00069 | 0.371 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.541 |
MOD_ProDKin_1 | 241 | 247 | PF00069 | 0.433 |
MOD_ProDKin_1 | 289 | 295 | PF00069 | 0.468 |
MOD_ProDKin_1 | 377 | 383 | PF00069 | 0.477 |
MOD_ProDKin_1 | 80 | 86 | PF00069 | 0.738 |
MOD_ProDKin_1 | 96 | 102 | PF00069 | 0.624 |
MOD_SUMO_rev_2 | 244 | 250 | PF00179 | 0.510 |
MOD_SUMO_rev_2 | 341 | 347 | PF00179 | 0.592 |
TRG_ENDOCYTIC_2 | 153 | 156 | PF00928 | 0.643 |
TRG_ENDOCYTIC_2 | 197 | 200 | PF00928 | 0.570 |
TRG_ENDOCYTIC_2 | 26 | 29 | PF00928 | 0.421 |
TRG_ENDOCYTIC_2 | 390 | 393 | PF00928 | 0.512 |
TRG_ER_diArg_1 | 143 | 146 | PF00400 | 0.625 |
TRG_ER_diArg_1 | 153 | 155 | PF00400 | 0.669 |
TRG_ER_diArg_1 | 167 | 169 | PF00400 | 0.634 |
TRG_ER_diArg_1 | 451 | 453 | PF00400 | 0.518 |
TRG_ER_diArg_1 | 51 | 54 | PF00400 | 0.567 |
TRG_Pf-PMV_PEXEL_1 | 363 | 367 | PF00026 | 0.552 |
TRG_Pf-PMV_PEXEL_1 | 468 | 473 | PF00026 | 0.512 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6I6 | Leptomonas seymouri | 54% | 100% |
A0A0S4JBB6 | Bodo saltans | 26% | 96% |
A0A1X0NPY5 | Trypanosomatidae | 37% | 100% |
A0A3R7KWR6 | Trypanosoma rangeli | 39% | 100% |
A0A3S7WSC4 | Leishmania donovani | 96% | 100% |
A4H722 | Leishmania braziliensis | 83% | 100% |
A4HVF1 | Leishmania infantum | 97% | 100% |
D0A6V8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
E9AP49 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
V5BDY2 | Trypanosoma cruzi | 39% | 100% |