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: E9AP49
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 321 | 325 | PF00656 | 0.467 |
CLV_NRD_NRD_1 | 136 | 138 | PF00675 | 0.644 |
CLV_NRD_NRD_1 | 146 | 148 | PF00675 | 0.583 |
CLV_NRD_NRD_1 | 154 | 156 | PF00675 | 0.636 |
CLV_NRD_NRD_1 | 167 | 169 | PF00675 | 0.623 |
CLV_NRD_NRD_1 | 435 | 437 | PF00675 | 0.460 |
CLV_PCSK_FUR_1 | 144 | 148 | PF00082 | 0.647 |
CLV_PCSK_KEX2_1 | 144 | 146 | PF00082 | 0.707 |
CLV_PCSK_KEX2_1 | 154 | 156 | PF00082 | 0.614 |
CLV_PCSK_KEX2_1 | 167 | 169 | PF00082 | 0.666 |
CLV_PCSK_KEX2_1 | 435 | 437 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 452 | 454 | PF00082 | 0.581 |
CLV_PCSK_PC1ET2_1 | 452 | 454 | PF00082 | 0.566 |
CLV_PCSK_SKI1_1 | 12 | 16 | PF00082 | 0.469 |
CLV_PCSK_SKI1_1 | 154 | 158 | PF00082 | 0.689 |
CLV_PCSK_SKI1_1 | 429 | 433 | PF00082 | 0.426 |
DEG_SPOP_SBC_1 | 103 | 107 | PF00917 | 0.785 |
DOC_CKS1_1 | 81 | 86 | PF01111 | 0.782 |
DOC_CKS1_1 | 97 | 102 | PF01111 | 0.518 |
DOC_MAPK_gen_1 | 137 | 143 | PF00069 | 0.618 |
DOC_MAPK_gen_1 | 21 | 31 | PF00069 | 0.287 |
DOC_PP4_FxxP_1 | 303 | 306 | PF00568 | 0.490 |
DOC_USP7_MATH_1 | 101 | 105 | PF00917 | 0.781 |
DOC_USP7_MATH_1 | 114 | 118 | PF00917 | 0.753 |
DOC_USP7_MATH_1 | 297 | 301 | PF00917 | 0.418 |
DOC_USP7_MATH_1 | 366 | 370 | PF00917 | 0.601 |
DOC_WW_Pin1_4 | 241 | 246 | PF00397 | 0.443 |
DOC_WW_Pin1_4 | 289 | 294 | PF00397 | 0.469 |
DOC_WW_Pin1_4 | 80 | 85 | PF00397 | 0.741 |
DOC_WW_Pin1_4 | 96 | 101 | PF00397 | 0.590 |
LIG_14-3-3_CanoR_1 | 137 | 143 | PF00244 | 0.672 |
LIG_14-3-3_CanoR_1 | 162 | 169 | PF00244 | 0.531 |
LIG_14-3-3_CanoR_1 | 339 | 343 | PF00244 | 0.587 |
LIG_14-3-3_CanoR_1 | 435 | 440 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 67 | 73 | PF00244 | 0.746 |
LIG_APCC_ABBA_1 | 275 | 280 | PF00400 | 0.388 |
LIG_BRCT_BRCA1_1 | 299 | 303 | PF00533 | 0.320 |
LIG_BRCT_BRCA1_1 | 419 | 423 | PF00533 | 0.218 |
LIG_deltaCOP1_diTrp_1 | 232 | 239 | PF00928 | 0.560 |
LIG_EH1_1 | 355 | 363 | PF00400 | 0.627 |
LIG_eIF4E_1 | 451 | 457 | PF01652 | 0.573 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.762 |
LIG_FHA_2 | 172 | 178 | PF00498 | 0.649 |
LIG_FHA_2 | 194 | 200 | PF00498 | 0.587 |
LIG_FHA_2 | 241 | 247 | PF00498 | 0.470 |
LIG_FHA_2 | 319 | 325 | PF00498 | 0.621 |
LIG_HP1_1 | 372 | 376 | PF01393 | 0.393 |
LIG_Integrin_RGD_1 | 54 | 56 | PF01839 | 0.612 |
LIG_LIR_Apic_2 | 300 | 306 | PF02991 | 0.539 |
LIG_LIR_Gen_1 | 196 | 204 | PF02991 | 0.573 |
LIG_LIR_Gen_1 | 236 | 245 | PF02991 | 0.417 |
LIG_LIR_Gen_1 | 420 | 431 | PF02991 | 0.227 |
LIG_LIR_Nem_3 | 13 | 18 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 150 | 156 | PF02991 | 0.611 |
LIG_LIR_Nem_3 | 196 | 200 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 236 | 240 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 295 | 299 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 420 | 426 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 460 | 466 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 56 | 62 | PF02991 | 0.601 |
LIG_MYND_1 | 377 | 381 | PF01753 | 0.533 |
LIG_Pex14_2 | 11 | 15 | PF04695 | 0.537 |
LIG_Pex14_2 | 229 | 233 | PF04695 | 0.602 |
LIG_RPA_C_Fungi | 140 | 152 | PF08784 | 0.430 |
LIG_SH2_CRK | 153 | 157 | PF00017 | 0.612 |
LIG_SH2_CRK | 26 | 30 | PF00017 | 0.473 |
LIG_SH2_STAP1 | 278 | 282 | PF00017 | 0.505 |
LIG_SH2_STAP1 | 421 | 425 | PF00017 | 0.372 |
LIG_SH2_STAT5 | 172 | 175 | PF00017 | 0.627 |
LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.693 |
LIG_SH2_STAT5 | 268 | 271 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 390 | 393 | PF00017 | 0.392 |
LIG_SH3_3 | 11 | 17 | PF00018 | 0.544 |
LIG_SH3_3 | 371 | 377 | PF00018 | 0.443 |
LIG_SH3_3 | 69 | 75 | PF00018 | 0.538 |
LIG_SH3_3 | 91 | 97 | PF00018 | 0.765 |
LIG_TRAF2_1 | 174 | 177 | PF00917 | 0.598 |
LIG_TRFH_1 | 423 | 427 | PF08558 | 0.207 |
MOD_CDK_SPxxK_3 | 241 | 248 | PF00069 | 0.489 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.748 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.618 |
MOD_CK1_1 | 207 | 213 | PF00069 | 0.575 |
MOD_CK1_1 | 289 | 295 | PF00069 | 0.557 |
MOD_CK1_1 | 320 | 326 | PF00069 | 0.585 |
MOD_CK1_1 | 438 | 444 | PF00069 | 0.477 |
MOD_CK2_1 | 171 | 177 | PF00069 | 0.647 |
MOD_CK2_1 | 240 | 246 | PF00069 | 0.510 |
MOD_CK2_1 | 278 | 284 | PF00069 | 0.465 |
MOD_Cter_Amidation | 433 | 436 | PF01082 | 0.522 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.594 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.584 |
MOD_GlcNHglycan | 280 | 283 | PF01048 | 0.509 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.538 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.609 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.547 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.561 |
MOD_GSK3_1 | 417 | 424 | PF00069 | 0.444 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.449 |
MOD_N-GLC_1 | 181 | 186 | PF02516 | 0.648 |
MOD_N-GLC_1 | 289 | 294 | PF02516 | 0.497 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.785 |
MOD_NEK2_1 | 200 | 205 | PF00069 | 0.683 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.509 |
MOD_NEK2_1 | 240 | 245 | PF00069 | 0.518 |
MOD_NEK2_1 | 392 | 397 | PF00069 | 0.491 |
MOD_NEK2_1 | 46 | 51 | PF00069 | 0.458 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.714 |
MOD_PIKK_1 | 131 | 137 | PF00454 | 0.477 |
MOD_PIKK_1 | 392 | 398 | PF00454 | 0.533 |
MOD_PKA_1 | 154 | 160 | PF00069 | 0.704 |
MOD_PKA_1 | 435 | 441 | PF00069 | 0.533 |
MOD_PKA_2 | 136 | 142 | PF00069 | 0.608 |
MOD_PKA_2 | 154 | 160 | PF00069 | 0.620 |
MOD_PKA_2 | 161 | 167 | PF00069 | 0.684 |
MOD_PKA_2 | 207 | 213 | PF00069 | 0.569 |
MOD_PKA_2 | 316 | 322 | PF00069 | 0.370 |
MOD_PKA_2 | 338 | 344 | PF00069 | 0.560 |
MOD_PKA_2 | 435 | 441 | PF00069 | 0.468 |
MOD_Plk_1 | 283 | 289 | PF00069 | 0.593 |
MOD_Plk_1 | 366 | 372 | PF00069 | 0.598 |
MOD_Plk_4 | 212 | 218 | PF00069 | 0.512 |
MOD_Plk_4 | 225 | 231 | PF00069 | 0.631 |
MOD_Plk_4 | 324 | 330 | PF00069 | 0.554 |
MOD_Plk_4 | 357 | 363 | PF00069 | 0.564 |
MOD_ProDKin_1 | 241 | 247 | PF00069 | 0.436 |
MOD_ProDKin_1 | 289 | 295 | PF00069 | 0.466 |
MOD_ProDKin_1 | 80 | 86 | PF00069 | 0.741 |
MOD_ProDKin_1 | 96 | 102 | PF00069 | 0.594 |
MOD_SUMO_rev_2 | 244 | 250 | PF00179 | 0.513 |
MOD_SUMO_rev_2 | 341 | 347 | PF00179 | 0.557 |
TRG_DiLeu_BaEn_2 | 224 | 230 | PF01217 | 0.375 |
TRG_ENDOCYTIC_2 | 153 | 156 | PF00928 | 0.646 |
TRG_ENDOCYTIC_2 | 197 | 200 | PF00928 | 0.553 |
TRG_ENDOCYTIC_2 | 26 | 29 | PF00928 | 0.415 |
TRG_ENDOCYTIC_2 | 390 | 393 | PF00928 | 0.505 |
TRG_ER_diArg_1 | 143 | 146 | PF00400 | 0.706 |
TRG_ER_diArg_1 | 153 | 155 | PF00400 | 0.703 |
TRG_ER_diArg_1 | 167 | 169 | PF00400 | 0.651 |
TRG_ER_diArg_1 | 51 | 54 | PF00400 | 0.571 |
TRG_Pf-PMV_PEXEL_1 | 363 | 367 | PF00026 | 0.547 |
TRG_Pf-PMV_PEXEL_1 | 468 | 473 | PF00026 | 0.513 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6I6 | Leptomonas seymouri | 53% | 100% |
A0A0S4JBB6 | Bodo saltans | 26% | 96% |
A0A1X0NPY5 | Trypanosomatidae | 37% | 100% |
A0A3R7KWR6 | Trypanosoma rangeli | 39% | 100% |
A0A3S7WSC4 | Leishmania donovani | 93% | 100% |
A4H722 | Leishmania braziliensis | 80% | 100% |
A4HVF1 | Leishmania infantum | 93% | 100% |
D0A6V8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
Q4QGD9 | Leishmania major | 93% | 100% |
V5BDY2 | Trypanosoma cruzi | 39% | 100% |