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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AM25
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 9 |
GO:0005488 | binding | 1 | 9 |
GO:0097159 | organic cyclic compound binding | 2 | 9 |
GO:1901363 | heterocyclic compound binding | 2 | 9 |
GO:0003824 | catalytic activity | 1 | 3 |
GO:0004518 | nuclease activity | 4 | 3 |
GO:0004527 | exonuclease activity | 5 | 3 |
GO:0016787 | hydrolase activity | 2 | 3 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 107 | 111 | PF00656 | 0.816 |
CLV_C14_Caspase3-7 | 135 | 139 | PF00656 | 0.744 |
CLV_C14_Caspase3-7 | 341 | 345 | PF00656 | 0.573 |
CLV_NRD_NRD_1 | 147 | 149 | PF00675 | 0.638 |
CLV_NRD_NRD_1 | 335 | 337 | PF00675 | 0.364 |
CLV_NRD_NRD_1 | 367 | 369 | PF00675 | 0.301 |
CLV_NRD_NRD_1 | 421 | 423 | PF00675 | 0.325 |
CLV_NRD_NRD_1 | 45 | 47 | PF00675 | 0.695 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.525 |
CLV_PCSK_KEX2_1 | 335 | 337 | PF00082 | 0.339 |
CLV_PCSK_KEX2_1 | 367 | 369 | PF00082 | 0.339 |
CLV_PCSK_KEX2_1 | 421 | 423 | PF00082 | 0.329 |
CLV_PCSK_PC1ET2_1 | 213 | 215 | PF00082 | 0.525 |
CLV_PCSK_PC7_1 | 209 | 215 | PF00082 | 0.615 |
CLV_PCSK_SKI1_1 | 117 | 121 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 148 | 152 | PF00082 | 0.711 |
CLV_PCSK_SKI1_1 | 213 | 217 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 40 | 44 | PF00082 | 0.689 |
CLV_PCSK_SKI1_1 | 403 | 407 | PF00082 | 0.314 |
CLV_PCSK_SKI1_1 | 497 | 501 | PF00082 | 0.692 |
DEG_APCC_DBOX_1 | 116 | 124 | PF00400 | 0.657 |
DEG_SPOP_SBC_1 | 78 | 82 | PF00917 | 0.745 |
DEG_SPOP_SBC_1 | 83 | 87 | PF00917 | 0.735 |
DOC_CYCLIN_yCln2_LP_2 | 216 | 222 | PF00134 | 0.466 |
DOC_MAPK_gen_1 | 412 | 418 | PF00069 | 0.482 |
DOC_PP4_FxxP_1 | 99 | 102 | PF00568 | 0.618 |
DOC_SPAK_OSR1_1 | 127 | 131 | PF12202 | 0.645 |
DOC_USP7_MATH_1 | 153 | 157 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 178 | 182 | PF00917 | 0.816 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.775 |
DOC_USP7_MATH_1 | 348 | 352 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 38 | 42 | PF00917 | 0.706 |
DOC_USP7_MATH_1 | 51 | 55 | PF00917 | 0.730 |
DOC_USP7_MATH_1 | 67 | 71 | PF00917 | 0.815 |
DOC_USP7_MATH_1 | 83 | 87 | PF00917 | 0.723 |
DOC_WW_Pin1_4 | 102 | 107 | PF00397 | 0.611 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.679 |
DOC_WW_Pin1_4 | 53 | 58 | PF00397 | 0.728 |
DOC_WW_Pin1_4 | 79 | 84 | PF00397 | 0.809 |
LIG_14-3-3_CanoR_1 | 180 | 184 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 27 | 35 | PF00244 | 0.723 |
LIG_14-3-3_CanoR_1 | 3 | 8 | PF00244 | 0.646 |
LIG_14-3-3_CanoR_1 | 393 | 397 | PF00244 | 0.499 |
LIG_14-3-3_CanoR_1 | 40 | 48 | PF00244 | 0.681 |
LIG_Actin_WH2_2 | 243 | 259 | PF00022 | 0.539 |
LIG_Actin_WH2_2 | 363 | 379 | PF00022 | 0.564 |
LIG_APCC_ABBAyCdc20_2 | 335 | 341 | PF00400 | 0.539 |
LIG_BRCT_BRCA1_1 | 396 | 400 | PF00533 | 0.602 |
LIG_BRCT_BRCA1_1 | 414 | 418 | PF00533 | 0.382 |
LIG_deltaCOP1_diTrp_1 | 361 | 369 | PF00928 | 0.499 |
LIG_FHA_1 | 251 | 257 | PF00498 | 0.499 |
LIG_FHA_1 | 406 | 412 | PF00498 | 0.499 |
LIG_FHA_1 | 427 | 433 | PF00498 | 0.539 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.566 |
LIG_FHA_2 | 348 | 354 | PF00498 | 0.516 |
LIG_FHA_2 | 69 | 75 | PF00498 | 0.742 |
LIG_HP1_1 | 247 | 251 | PF01393 | 0.539 |
LIG_Integrin_RGD_1 | 175 | 177 | PF01839 | 0.619 |
LIG_Integrin_RGD_1 | 457 | 459 | PF01839 | 0.627 |
LIG_LIR_Apic_2 | 96 | 102 | PF02991 | 0.616 |
LIG_LIR_Gen_1 | 126 | 132 | PF02991 | 0.645 |
LIG_LIR_Nem_3 | 126 | 131 | PF02991 | 0.643 |
LIG_LIR_Nem_3 | 245 | 249 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 261 | 265 | PF02991 | 0.484 |
LIG_MYND_1 | 102 | 106 | PF01753 | 0.525 |
LIG_PCNA_yPIPBox_3 | 401 | 411 | PF02747 | 0.539 |
LIG_Pex14_1 | 317 | 321 | PF04695 | 0.539 |
LIG_SH2_CRK | 387 | 391 | PF00017 | 0.539 |
LIG_SH2_GRB2like | 389 | 392 | PF00017 | 0.539 |
LIG_SH2_PTP2 | 265 | 268 | PF00017 | 0.474 |
LIG_SH2_PTP2 | 389 | 392 | PF00017 | 0.539 |
LIG_SH2_SRC | 339 | 342 | PF00017 | 0.517 |
LIG_SH2_SRC | 389 | 392 | PF00017 | 0.539 |
LIG_SH2_STAP1 | 396 | 400 | PF00017 | 0.539 |
LIG_SH2_STAT5 | 265 | 268 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 389 | 392 | PF00017 | 0.539 |
LIG_SH3_3 | 193 | 199 | PF00018 | 0.721 |
LIG_SH3_3 | 20 | 26 | PF00018 | 0.689 |
LIG_SH3_3 | 204 | 210 | PF00018 | 0.738 |
LIG_SH3_3 | 234 | 240 | PF00018 | 0.499 |
LIG_SH3_3 | 288 | 294 | PF00018 | 0.489 |
LIG_SH3_3 | 377 | 383 | PF00018 | 0.564 |
LIG_SUMO_SIM_par_1 | 245 | 253 | PF11976 | 0.509 |
LIG_SUMO_SIM_par_1 | 287 | 293 | PF11976 | 0.556 |
LIG_SxIP_EBH_1 | 199 | 213 | PF03271 | 0.648 |
LIG_TRAF2_1 | 168 | 171 | PF00917 | 0.704 |
LIG_TRAF2_1 | 467 | 470 | PF00917 | 0.639 |
LIG_TRAF2_2 | 172 | 177 | PF00917 | 0.512 |
LIG_TYR_ITIM | 385 | 390 | PF00017 | 0.484 |
LIG_WW_3 | 24 | 28 | PF00397 | 0.685 |
MOD_CDK_SPK_2 | 53 | 58 | PF00069 | 0.744 |
MOD_CDK_SPxxK_3 | 102 | 109 | PF00069 | 0.522 |
MOD_CK1_1 | 105 | 111 | PF00069 | 0.644 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.790 |
MOD_CK1_1 | 52 | 58 | PF00069 | 0.800 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.693 |
MOD_CK2_1 | 179 | 185 | PF00069 | 0.741 |
MOD_CK2_1 | 27 | 33 | PF00069 | 0.511 |
MOD_CK2_1 | 347 | 353 | PF00069 | 0.568 |
MOD_CK2_1 | 68 | 74 | PF00069 | 0.697 |
MOD_Cter_Amidation | 419 | 422 | PF01082 | 0.339 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.782 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.695 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.274 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.364 |
MOD_GlcNHglycan | 40 | 43 | PF01048 | 0.716 |
MOD_GlcNHglycan | 423 | 426 | PF01048 | 0.287 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.779 |
MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.784 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.684 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.624 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.686 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.474 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.716 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.747 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.754 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.678 |
MOD_N-GLC_1 | 348 | 353 | PF02516 | 0.381 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.664 |
MOD_NEK2_1 | 132 | 137 | PF00069 | 0.623 |
MOD_NEK2_1 | 200 | 205 | PF00069 | 0.725 |
MOD_NEK2_1 | 228 | 233 | PF00069 | 0.539 |
MOD_NEK2_2 | 233 | 238 | PF00069 | 0.539 |
MOD_OFUCOSY | 226 | 232 | PF10250 | 0.299 |
MOD_PIKK_1 | 142 | 148 | PF00454 | 0.747 |
MOD_PIKK_1 | 166 | 172 | PF00454 | 0.776 |
MOD_PIKK_1 | 282 | 288 | PF00454 | 0.485 |
MOD_PKA_1 | 148 | 154 | PF00069 | 0.744 |
MOD_PKA_1 | 412 | 418 | PF00069 | 0.488 |
MOD_PKA_1 | 421 | 427 | PF00069 | 0.479 |
MOD_PKA_2 | 179 | 185 | PF00069 | 0.547 |
MOD_PKA_2 | 201 | 207 | PF00069 | 0.482 |
MOD_PKA_2 | 324 | 330 | PF00069 | 0.525 |
MOD_PKA_2 | 392 | 398 | PF00069 | 0.493 |
MOD_PKA_2 | 421 | 427 | PF00069 | 0.501 |
MOD_Plk_1 | 178 | 184 | PF00069 | 0.660 |
MOD_Plk_1 | 371 | 377 | PF00069 | 0.477 |
MOD_Plk_2-3 | 179 | 185 | PF00069 | 0.687 |
MOD_Plk_4 | 179 | 185 | PF00069 | 0.770 |
MOD_Plk_4 | 294 | 300 | PF00069 | 0.517 |
MOD_Plk_4 | 371 | 377 | PF00069 | 0.499 |
MOD_ProDKin_1 | 102 | 108 | PF00069 | 0.609 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.681 |
MOD_ProDKin_1 | 53 | 59 | PF00069 | 0.726 |
MOD_ProDKin_1 | 79 | 85 | PF00069 | 0.809 |
MOD_SUMO_for_1 | 306 | 309 | PF00179 | 0.517 |
MOD_SUMO_for_1 | 330 | 333 | PF00179 | 0.539 |
TRG_DiLeu_BaEn_1 | 179 | 184 | PF01217 | 0.689 |
TRG_DiLeu_BaEn_2 | 332 | 338 | PF01217 | 0.539 |
TRG_DiLeu_BaLyEn_6 | 211 | 216 | PF01217 | 0.593 |
TRG_ENDOCYTIC_2 | 387 | 390 | PF00928 | 0.484 |
TRG_ER_diArg_1 | 2 | 5 | PF00400 | 0.623 |
TRG_ER_diArg_1 | 335 | 337 | PF00400 | 0.564 |
TRG_ER_diArg_1 | 366 | 368 | PF00400 | 0.539 |
TRG_Pf-PMV_PEXEL_1 | 12 | 17 | PF00026 | 0.547 |
TRG_Pf-PMV_PEXEL_1 | 214 | 218 | PF00026 | 0.454 |
TRG_Pf-PMV_PEXEL_1 | 434 | 438 | PF00026 | 0.299 |
TRG_Pf-PMV_PEXEL_1 | 5 | 10 | PF00026 | 0.581 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7G3 | Leptomonas seymouri | 60% | 95% |
A0A0S4JDV1 | Bodo saltans | 36% | 100% |
A0A3R7M512 | Trypanosoma rangeli | 50% | 100% |
A0A3S7X262 | Leishmania donovani | 94% | 100% |
A4HH55 | Leishmania braziliensis | 79% | 100% |
A4I4A6 | Leishmania infantum | 93% | 100% |
E9ADQ5 | Leishmania major | 92% | 100% |