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: 18 |
NetGPI | no | yes: 0, no: 18 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005739 | mitochondrion | 5 | 1 |
GO:0020023 | kinetoplast | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HHF5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 318 | 322 | PF00656 | 0.537 |
CLV_NRD_NRD_1 | 187 | 189 | PF00675 | 0.396 |
CLV_NRD_NRD_1 | 478 | 480 | PF00675 | 0.579 |
CLV_NRD_NRD_1 | 486 | 488 | PF00675 | 0.541 |
CLV_NRD_NRD_1 | 64 | 66 | PF00675 | 0.678 |
CLV_NRD_NRD_1 | 7 | 9 | PF00675 | 0.755 |
CLV_PCSK_KEX2_1 | 104 | 106 | PF00082 | 0.411 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.578 |
CLV_PCSK_KEX2_1 | 187 | 189 | PF00082 | 0.414 |
CLV_PCSK_KEX2_1 | 367 | 369 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 486 | 488 | PF00082 | 0.574 |
CLV_PCSK_KEX2_1 | 7 | 9 | PF00082 | 0.755 |
CLV_PCSK_PC1ET2_1 | 104 | 106 | PF00082 | 0.408 |
CLV_PCSK_PC1ET2_1 | 142 | 144 | PF00082 | 0.708 |
CLV_PCSK_PC1ET2_1 | 367 | 369 | PF00082 | 0.557 |
CLV_PCSK_PC7_1 | 3 | 9 | PF00082 | 0.656 |
CLV_PCSK_PC7_1 | 482 | 488 | PF00082 | 0.550 |
CLV_PCSK_SKI1_1 | 157 | 161 | PF00082 | 0.605 |
CLV_PCSK_SKI1_1 | 341 | 345 | PF00082 | 0.349 |
CLV_PCSK_SKI1_1 | 348 | 352 | PF00082 | 0.419 |
DEG_APCC_DBOX_1 | 187 | 195 | PF00400 | 0.455 |
DEG_APCC_DBOX_1 | 340 | 348 | PF00400 | 0.408 |
DEG_APCC_DBOX_1 | 7 | 15 | PF00400 | 0.502 |
DEG_SCF_FBW7_1 | 148 | 154 | PF00400 | 0.443 |
DEG_SCF_FBW7_1 | 440 | 445 | PF00400 | 0.564 |
DOC_ANK_TNKS_1 | 231 | 238 | PF00023 | 0.417 |
DOC_CKS1_1 | 148 | 153 | PF01111 | 0.678 |
DOC_CYCLIN_yCln2_LP_2 | 210 | 216 | PF00134 | 0.261 |
DOC_MAPK_gen_1 | 104 | 110 | PF00069 | 0.440 |
DOC_MAPK_gen_1 | 157 | 165 | PF00069 | 0.624 |
DOC_MAPK_gen_1 | 187 | 195 | PF00069 | 0.485 |
DOC_MAPK_gen_1 | 65 | 73 | PF00069 | 0.752 |
DOC_MAPK_gen_1 | 7 | 13 | PF00069 | 0.536 |
DOC_MAPK_MEF2A_6 | 104 | 112 | PF00069 | 0.383 |
DOC_MAPK_MEF2A_6 | 187 | 195 | PF00069 | 0.485 |
DOC_MAPK_MEF2A_6 | 66 | 75 | PF00069 | 0.484 |
DOC_MAPK_NFAT4_5 | 105 | 113 | PF00069 | 0.391 |
DOC_MAPK_NFAT4_5 | 188 | 196 | PF00069 | 0.485 |
DOC_PP1_RVXF_1 | 396 | 402 | PF00149 | 0.308 |
DOC_PP2B_LxvP_1 | 163 | 166 | PF13499 | 0.572 |
DOC_PP2B_LxvP_1 | 210 | 213 | PF13499 | 0.271 |
DOC_USP7_MATH_1 | 285 | 289 | PF00917 | 0.557 |
DOC_USP7_MATH_1 | 331 | 335 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 424 | 428 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 61 | 65 | PF00917 | 0.716 |
DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.502 |
DOC_WW_Pin1_4 | 147 | 152 | PF00397 | 0.642 |
DOC_WW_Pin1_4 | 164 | 169 | PF00397 | 0.618 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.529 |
DOC_WW_Pin1_4 | 204 | 209 | PF00397 | 0.477 |
DOC_WW_Pin1_4 | 319 | 324 | PF00397 | 0.492 |
DOC_WW_Pin1_4 | 354 | 359 | PF00397 | 0.518 |
DOC_WW_Pin1_4 | 428 | 433 | PF00397 | 0.723 |
DOC_WW_Pin1_4 | 438 | 443 | PF00397 | 0.536 |
DOC_WW_Pin1_4 | 493 | 498 | PF00397 | 0.727 |
DOC_WW_Pin1_4 | 50 | 55 | PF00397 | 0.629 |
LIG_14-3-3_CanoR_1 | 19 | 25 | PF00244 | 0.688 |
LIG_14-3-3_CanoR_1 | 240 | 249 | PF00244 | 0.358 |
LIG_14-3-3_CanoR_1 | 32 | 39 | PF00244 | 0.558 |
LIG_14-3-3_CanoR_1 | 333 | 340 | PF00244 | 0.545 |
LIG_14-3-3_CanoR_1 | 381 | 389 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 391 | 399 | PF00244 | 0.378 |
LIG_14-3-3_CanoR_1 | 433 | 442 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 65 | 69 | PF00244 | 0.768 |
LIG_14-3-3_CterR_2 | 500 | 505 | PF00244 | 0.481 |
LIG_Actin_WH2_2 | 332 | 350 | PF00022 | 0.490 |
LIG_AP2alpha_1 | 175 | 179 | PF02296 | 0.447 |
LIG_APCC_ABBA_1 | 172 | 177 | PF00400 | 0.580 |
LIG_APCC_ABBA_1 | 220 | 225 | PF00400 | 0.495 |
LIG_BIR_III_2 | 355 | 359 | PF00653 | 0.354 |
LIG_BIR_III_4 | 300 | 304 | PF00653 | 0.557 |
LIG_deltaCOP1_diTrp_1 | 127 | 136 | PF00928 | 0.606 |
LIG_deltaCOP1_diTrp_1 | 78 | 87 | PF00928 | 0.483 |
LIG_eIF4E_1 | 452 | 458 | PF01652 | 0.447 |
LIG_EVH1_2 | 212 | 216 | PF00568 | 0.346 |
LIG_EVH1_2 | 359 | 363 | PF00568 | 0.485 |
LIG_FHA_1 | 19 | 25 | PF00498 | 0.723 |
LIG_FHA_1 | 205 | 211 | PF00498 | 0.337 |
LIG_FHA_1 | 250 | 256 | PF00498 | 0.342 |
LIG_FHA_1 | 300 | 306 | PF00498 | 0.587 |
LIG_FHA_1 | 435 | 441 | PF00498 | 0.673 |
LIG_Integrin_RGD_1 | 181 | 183 | PF01839 | 0.466 |
LIG_LIR_Gen_1 | 127 | 136 | PF02991 | 0.594 |
LIG_LIR_Gen_1 | 173 | 184 | PF02991 | 0.544 |
LIG_LIR_Gen_1 | 290 | 297 | PF02991 | 0.391 |
LIG_LIR_Gen_1 | 386 | 396 | PF02991 | 0.444 |
LIG_LIR_Gen_1 | 78 | 85 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 127 | 133 | PF02991 | 0.610 |
LIG_LIR_Nem_3 | 173 | 179 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 290 | 295 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 386 | 392 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 78 | 84 | PF02991 | 0.476 |
LIG_MYND_1 | 208 | 212 | PF01753 | 0.292 |
LIG_NRBOX | 190 | 196 | PF00104 | 0.485 |
LIG_Pex14_2 | 175 | 179 | PF04695 | 0.579 |
LIG_SH2_GRB2like | 197 | 200 | PF00017 | 0.512 |
LIG_SH2_GRB2like | 452 | 455 | PF00017 | 0.519 |
LIG_SH2_SRC | 164 | 167 | PF00017 | 0.579 |
LIG_SH2_STAT5 | 140 | 143 | PF00017 | 0.680 |
LIG_SH2_STAT5 | 164 | 167 | PF00017 | 0.521 |
LIG_SH2_STAT5 | 197 | 200 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 371 | 374 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 395 | 398 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 452 | 455 | PF00017 | 0.636 |
LIG_SH3_1 | 145 | 151 | PF00018 | 0.546 |
LIG_SH3_1 | 487 | 493 | PF00018 | 0.536 |
LIG_SH3_1 | 57 | 63 | PF00018 | 0.528 |
LIG_SH3_2 | 60 | 65 | PF14604 | 0.521 |
LIG_SH3_3 | 145 | 151 | PF00018 | 0.696 |
LIG_SH3_3 | 162 | 168 | PF00018 | 0.407 |
LIG_SH3_3 | 487 | 493 | PF00018 | 0.784 |
LIG_SH3_3 | 57 | 63 | PF00018 | 0.825 |
LIG_TRAF2_1 | 288 | 291 | PF00917 | 0.596 |
LIG_UBA3_1 | 113 | 121 | PF00899 | 0.313 |
LIG_WRC_WIRS_1 | 292 | 297 | PF05994 | 0.397 |
MOD_CDK_SPK_2 | 2 | 7 | PF00069 | 0.487 |
MOD_CDK_SPK_2 | 428 | 433 | PF00069 | 0.457 |
MOD_CDK_SPK_2 | 52 | 57 | PF00069 | 0.616 |
MOD_CDK_SPxK_1 | 2 | 8 | PF00069 | 0.526 |
MOD_CDK_SPxxK_3 | 493 | 500 | PF00069 | 0.568 |
MOD_CDK_SPxxK_3 | 50 | 57 | PF00069 | 0.617 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.621 |
MOD_CK1_1 | 284 | 290 | PF00069 | 0.530 |
MOD_CK1_1 | 322 | 328 | PF00069 | 0.571 |
MOD_CK1_1 | 468 | 474 | PF00069 | 0.613 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.680 |
MOD_CK1_1 | 64 | 70 | PF00069 | 0.558 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.516 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.609 |
MOD_CK2_1 | 284 | 290 | PF00069 | 0.518 |
MOD_CK2_1 | 76 | 82 | PF00069 | 0.632 |
MOD_Cter_Amidation | 102 | 105 | PF01082 | 0.429 |
MOD_Cter_Amidation | 484 | 487 | PF01082 | 0.519 |
MOD_DYRK1A_RPxSP_1 | 428 | 432 | PF00069 | 0.691 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.389 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.670 |
MOD_GlcNHglycan | 283 | 286 | PF01048 | 0.501 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.596 |
MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.484 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.705 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.496 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.565 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.778 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.652 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.583 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.587 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.659 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.624 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.748 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.565 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.577 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.710 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.573 |
MOD_N-GLC_1 | 462 | 467 | PF02516 | 0.701 |
MOD_N-GLC_2 | 199 | 201 | PF02516 | 0.278 |
MOD_NEK2_1 | 117 | 122 | PF00069 | 0.515 |
MOD_NEK2_1 | 462 | 467 | PF00069 | 0.679 |
MOD_NEK2_1 | 498 | 503 | PF00069 | 0.668 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.551 |
MOD_PIKK_1 | 434 | 440 | PF00454 | 0.762 |
MOD_PKA_2 | 18 | 24 | PF00069 | 0.746 |
MOD_PKA_2 | 390 | 396 | PF00069 | 0.363 |
MOD_PKA_2 | 49 | 55 | PF00069 | 0.688 |
MOD_PKA_2 | 64 | 70 | PF00069 | 0.670 |
MOD_Plk_1 | 326 | 332 | PF00069 | 0.484 |
MOD_Plk_1 | 468 | 474 | PF00069 | 0.568 |
MOD_Plk_2-3 | 316 | 322 | PF00069 | 0.485 |
MOD_Plk_4 | 113 | 119 | PF00069 | 0.501 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.440 |
MOD_Plk_4 | 268 | 274 | PF00069 | 0.520 |
MOD_Plk_4 | 76 | 82 | PF00069 | 0.569 |
MOD_ProDKin_1 | 147 | 153 | PF00069 | 0.640 |
MOD_ProDKin_1 | 164 | 170 | PF00069 | 0.617 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.531 |
MOD_ProDKin_1 | 204 | 210 | PF00069 | 0.481 |
MOD_ProDKin_1 | 319 | 325 | PF00069 | 0.481 |
MOD_ProDKin_1 | 354 | 360 | PF00069 | 0.527 |
MOD_ProDKin_1 | 428 | 434 | PF00069 | 0.722 |
MOD_ProDKin_1 | 438 | 444 | PF00069 | 0.538 |
MOD_ProDKin_1 | 493 | 499 | PF00069 | 0.727 |
MOD_ProDKin_1 | 50 | 56 | PF00069 | 0.628 |
TRG_DiLeu_BaEn_1 | 189 | 194 | PF01217 | 0.493 |
TRG_DiLeu_BaLyEn_6 | 154 | 159 | PF01217 | 0.626 |
TRG_DiLeu_BaLyEn_6 | 378 | 383 | PF01217 | 0.476 |
TRG_ENDOCYTIC_2 | 176 | 179 | PF00928 | 0.543 |
TRG_ER_diArg_1 | 6 | 8 | PF00400 | 0.708 |
TRG_NES_CRM1_1 | 260 | 274 | PF08389 | 0.407 |
TRG_NLS_MonoCore_2 | 141 | 146 | PF00514 | 0.468 |
TRG_Pf-PMV_PEXEL_1 | 121 | 125 | PF00026 | 0.484 |
TRG_Pf-PMV_PEXEL_1 | 157 | 161 | PF00026 | 0.506 |
TRG_Pf-PMV_PEXEL_1 | 381 | 386 | PF00026 | 0.340 |
TRG_Pf-PMV_PEXEL_1 | 433 | 438 | PF00026 | 0.567 |
TRG_Pf-PMV_PEXEL_1 | 7 | 12 | PF00026 | 0.502 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P950 | Leptomonas seymouri | 43% | 90% |
A0A0N1ILX4 | Leptomonas seymouri | 24% | 100% |
A0A1X0NZT5 | Trypanosomatidae | 30% | 100% |
A0A3Q8IAB6 | Leishmania donovani | 25% | 93% |
A0A3R7KFA4 | Trypanosoma rangeli | 30% | 100% |
A0A3S5IRP3 | Trypanosoma rangeli | 24% | 100% |
A0A3S7X2J5 | Leishmania donovani | 81% | 94% |
A4H889 | Leishmania braziliensis | 26% | 100% |
A4HWL2 | Leishmania infantum | 25% | 93% |
A4I4K3 | Leishmania infantum | 81% | 94% |
C9ZL87 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
C9ZXS8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
E9AE02 | Leishmania major | 81% | 100% |
E9ALT0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
E9AQB9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
Q4QF55 | Leishmania major | 26% | 100% |
V5D9T1 | Trypanosoma cruzi | 31% | 100% |