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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S7X262
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 8 |
GO:0003824 | catalytic activity | 1 | 3 |
GO:0004518 | nuclease activity | 4 | 3 |
GO:0004527 | exonuclease activity | 5 | 3 |
GO:0005488 | binding | 1 | 8 |
GO:0016787 | hydrolase activity | 2 | 3 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 3 |
GO:0097159 | organic cyclic compound binding | 2 | 8 |
GO:1901363 | heterocyclic compound binding | 2 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 107 | 111 | PF00656 | 0.705 |
CLV_C14_Caspase3-7 | 135 | 139 | PF00656 | 0.672 |
CLV_C14_Caspase3-7 | 341 | 345 | PF00656 | 0.517 |
CLV_NRD_NRD_1 | 142 | 144 | PF00675 | 0.636 |
CLV_NRD_NRD_1 | 147 | 149 | PF00675 | 0.640 |
CLV_NRD_NRD_1 | 335 | 337 | PF00675 | 0.332 |
CLV_NRD_NRD_1 | 367 | 369 | PF00675 | 0.293 |
CLV_NRD_NRD_1 | 421 | 423 | PF00675 | 0.297 |
CLV_NRD_NRD_1 | 45 | 47 | PF00675 | 0.648 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 335 | 337 | PF00082 | 0.265 |
CLV_PCSK_KEX2_1 | 367 | 369 | PF00082 | 0.333 |
CLV_PCSK_KEX2_1 | 421 | 423 | PF00082 | 0.306 |
CLV_PCSK_KEX2_1 | 500 | 502 | PF00082 | 0.671 |
CLV_PCSK_PC1ET2_1 | 213 | 215 | PF00082 | 0.481 |
CLV_PCSK_PC1ET2_1 | 500 | 502 | PF00082 | 0.641 |
CLV_PCSK_PC7_1 | 209 | 215 | PF00082 | 0.578 |
CLV_PCSK_SKI1_1 | 148 | 152 | PF00082 | 0.660 |
CLV_PCSK_SKI1_1 | 213 | 217 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 40 | 44 | PF00082 | 0.744 |
CLV_PCSK_SKI1_1 | 403 | 407 | PF00082 | 0.296 |
CLV_PCSK_SKI1_1 | 485 | 489 | PF00082 | 0.734 |
CLV_PCSK_SKI1_1 | 497 | 501 | PF00082 | 0.636 |
DEG_APCC_DBOX_1 | 116 | 124 | PF00400 | 0.606 |
DEG_SPOP_SBC_1 | 163 | 167 | PF00917 | 0.569 |
DEG_SPOP_SBC_1 | 78 | 82 | PF00917 | 0.690 |
DEG_SPOP_SBC_1 | 83 | 87 | PF00917 | 0.651 |
DOC_ANK_TNKS_1 | 174 | 181 | PF00023 | 0.567 |
DOC_CYCLIN_yCln2_LP_2 | 216 | 222 | PF00134 | 0.406 |
DOC_MAPK_gen_1 | 412 | 418 | PF00069 | 0.448 |
DOC_PP4_FxxP_1 | 99 | 102 | PF00568 | 0.597 |
DOC_SPAK_OSR1_1 | 127 | 131 | PF12202 | 0.593 |
DOC_USP7_MATH_1 | 153 | 157 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 178 | 182 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.466 |
DOC_USP7_MATH_1 | 348 | 352 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 38 | 42 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 51 | 55 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 77 | 81 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 83 | 87 | PF00917 | 0.637 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.618 |
DOC_WW_Pin1_4 | 53 | 58 | PF00397 | 0.683 |
DOC_WW_Pin1_4 | 79 | 84 | PF00397 | 0.736 |
LIG_14-3-3_CanoR_1 | 115 | 121 | PF00244 | 0.614 |
LIG_14-3-3_CanoR_1 | 3 | 8 | PF00244 | 0.587 |
LIG_14-3-3_CanoR_1 | 393 | 397 | PF00244 | 0.463 |
LIG_14-3-3_CanoR_1 | 40 | 48 | PF00244 | 0.622 |
LIG_Actin_WH2_2 | 243 | 259 | PF00022 | 0.506 |
LIG_Actin_WH2_2 | 363 | 379 | PF00022 | 0.517 |
LIG_APCC_ABBAyCdc20_2 | 335 | 341 | PF00400 | 0.506 |
LIG_BIR_III_4 | 177 | 181 | PF00653 | 0.568 |
LIG_BRCT_BRCA1_1 | 396 | 400 | PF00533 | 0.517 |
LIG_BRCT_BRCA1_1 | 414 | 418 | PF00533 | 0.385 |
LIG_deltaCOP1_diTrp_1 | 361 | 369 | PF00928 | 0.463 |
LIG_FHA_1 | 251 | 257 | PF00498 | 0.475 |
LIG_FHA_1 | 406 | 412 | PF00498 | 0.463 |
LIG_FHA_1 | 427 | 433 | PF00498 | 0.506 |
LIG_FHA_2 | 348 | 354 | PF00498 | 0.550 |
LIG_FHA_2 | 69 | 75 | PF00498 | 0.637 |
LIG_HP1_1 | 247 | 251 | PF01393 | 0.506 |
LIG_Integrin_RGD_1 | 175 | 177 | PF01839 | 0.584 |
LIG_Integrin_RGD_1 | 457 | 459 | PF01839 | 0.552 |
LIG_LIR_Apic_2 | 96 | 102 | PF02991 | 0.593 |
LIG_LIR_Gen_1 | 126 | 132 | PF02991 | 0.592 |
LIG_LIR_Nem_3 | 126 | 131 | PF02991 | 0.591 |
LIG_LIR_Nem_3 | 245 | 249 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 261 | 265 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 381 | 385 | PF02991 | 0.498 |
LIG_PCNA_yPIPBox_3 | 401 | 411 | PF02747 | 0.506 |
LIG_Pex14_1 | 317 | 321 | PF04695 | 0.506 |
LIG_SH2_CRK | 387 | 391 | PF00017 | 0.506 |
LIG_SH2_GRB2like | 389 | 392 | PF00017 | 0.506 |
LIG_SH2_PTP2 | 265 | 268 | PF00017 | 0.463 |
LIG_SH2_PTP2 | 389 | 392 | PF00017 | 0.506 |
LIG_SH2_SRC | 339 | 342 | PF00017 | 0.483 |
LIG_SH2_SRC | 389 | 392 | PF00017 | 0.506 |
LIG_SH2_STAP1 | 396 | 400 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 265 | 268 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 389 | 392 | PF00017 | 0.506 |
LIG_SH3_3 | 193 | 199 | PF00018 | 0.672 |
LIG_SH3_3 | 20 | 26 | PF00018 | 0.642 |
LIG_SH3_3 | 204 | 210 | PF00018 | 0.543 |
LIG_SH3_3 | 234 | 240 | PF00018 | 0.506 |
LIG_SH3_3 | 288 | 294 | PF00018 | 0.496 |
LIG_SH3_3 | 377 | 383 | PF00018 | 0.517 |
LIG_SH3_3 | 45 | 51 | PF00018 | 0.668 |
LIG_SUMO_SIM_par_1 | 245 | 253 | PF11976 | 0.506 |
LIG_SUMO_SIM_par_1 | 287 | 293 | PF11976 | 0.527 |
LIG_SxIP_EBH_1 | 199 | 213 | PF03271 | 0.602 |
LIG_TRAF2_1 | 168 | 171 | PF00917 | 0.613 |
LIG_TRAF2_1 | 467 | 470 | PF00917 | 0.569 |
LIG_TYR_ITIM | 385 | 390 | PF00017 | 0.463 |
LIG_WW_3 | 24 | 28 | PF00397 | 0.640 |
MOD_CDK_SPK_2 | 53 | 58 | PF00069 | 0.680 |
MOD_CK1_1 | 105 | 111 | PF00069 | 0.626 |
MOD_CK1_1 | 116 | 122 | PF00069 | 0.586 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.720 |
MOD_CK1_1 | 52 | 58 | PF00069 | 0.755 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.729 |
MOD_CK2_1 | 179 | 185 | PF00069 | 0.691 |
MOD_CK2_1 | 347 | 353 | PF00069 | 0.550 |
MOD_CK2_1 | 68 | 74 | PF00069 | 0.819 |
MOD_Cter_Amidation | 419 | 422 | PF01082 | 0.306 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.683 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.603 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.263 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.774 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.317 |
MOD_GlcNHglycan | 40 | 43 | PF01048 | 0.643 |
MOD_GlcNHglycan | 423 | 426 | PF01048 | 0.263 |
MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.737 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.700 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.759 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.609 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.477 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.686 |
MOD_GSK3_1 | 481 | 488 | PF00069 | 0.569 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.763 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.714 |
MOD_N-GLC_1 | 348 | 353 | PF02516 | 0.317 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.639 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.625 |
MOD_NEK2_1 | 132 | 137 | PF00069 | 0.595 |
MOD_NEK2_1 | 200 | 205 | PF00069 | 0.625 |
MOD_NEK2_1 | 228 | 233 | PF00069 | 0.506 |
MOD_NEK2_2 | 233 | 238 | PF00069 | 0.506 |
MOD_OFUCOSY | 226 | 232 | PF10250 | 0.263 |
MOD_PIKK_1 | 142 | 148 | PF00454 | 0.677 |
MOD_PIKK_1 | 166 | 172 | PF00454 | 0.703 |
MOD_PIKK_1 | 282 | 288 | PF00454 | 0.463 |
MOD_PKA_1 | 148 | 154 | PF00069 | 0.793 |
MOD_PKA_1 | 412 | 418 | PF00069 | 0.487 |
MOD_PKA_1 | 421 | 427 | PF00069 | 0.468 |
MOD_PKA_2 | 102 | 108 | PF00069 | 0.625 |
MOD_PKA_2 | 116 | 122 | PF00069 | 0.608 |
MOD_PKA_2 | 142 | 148 | PF00069 | 0.647 |
MOD_PKA_2 | 324 | 330 | PF00069 | 0.489 |
MOD_PKA_2 | 392 | 398 | PF00069 | 0.463 |
MOD_PKA_2 | 421 | 427 | PF00069 | 0.493 |
MOD_Plk_1 | 371 | 377 | PF00069 | 0.444 |
MOD_Plk_2-3 | 179 | 185 | PF00069 | 0.641 |
MOD_Plk_4 | 116 | 122 | PF00069 | 0.608 |
MOD_Plk_4 | 179 | 185 | PF00069 | 0.702 |
MOD_Plk_4 | 294 | 300 | PF00069 | 0.483 |
MOD_Plk_4 | 371 | 377 | PF00069 | 0.463 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.621 |
MOD_ProDKin_1 | 53 | 59 | PF00069 | 0.683 |
MOD_ProDKin_1 | 79 | 85 | PF00069 | 0.738 |
MOD_SUMO_for_1 | 306 | 309 | PF00179 | 0.483 |
MOD_SUMO_for_1 | 330 | 333 | PF00179 | 0.506 |
TRG_DiLeu_BaEn_1 | 179 | 184 | PF01217 | 0.642 |
TRG_DiLeu_BaEn_2 | 332 | 338 | PF01217 | 0.506 |
TRG_DiLeu_BaLyEn_6 | 211 | 216 | PF01217 | 0.546 |
TRG_ENDOCYTIC_2 | 387 | 390 | PF00928 | 0.463 |
TRG_ER_diArg_1 | 335 | 337 | PF00400 | 0.517 |
TRG_ER_diArg_1 | 366 | 368 | PF00400 | 0.533 |
TRG_Pf-PMV_PEXEL_1 | 12 | 17 | PF00026 | 0.577 |
TRG_Pf-PMV_PEXEL_1 | 214 | 218 | PF00026 | 0.406 |
TRG_Pf-PMV_PEXEL_1 | 434 | 438 | PF00026 | 0.263 |
TRG_Pf-PMV_PEXEL_1 | 5 | 10 | PF00026 | 0.568 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7G3 | Leptomonas seymouri | 61% | 95% |
A0A3R7M512 | Trypanosoma rangeli | 50% | 100% |
A4HH55 | Leishmania braziliensis | 79% | 100% |
A4I4A6 | Leishmania infantum | 100% | 100% |
E9ADQ5 | Leishmania major | 94% | 100% |
E9AM25 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |